Bi7250 Medical genetics and genetic counseling
Faculty of ScienceSpring 2025
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer)
doc. RNDr. Petr Kuglík, CSc. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 12 fields of study the course is directly associated with, display
- Course objectives
- The aim of this course is to provide a basic insight into human genetics and to familiarise students with basic principles and methods of medical genetics.
- Learning outcomes
- At the end of the course, students should be able to understand the principles of medical genetics; to describe and explain methods used in medical genetics; to apply learned knowledge for solving model examples in clinical medicine.
- Syllabus
- 1. Medical genetics and genetic counselling. 2. Etics and law in medical genetics. 3. Rare diseases. 4. Preventive approach in medical genetics, primary and secondary prevention. 5. New approaches in human cytogenetics. Genetics of disorders of intellectual development. 6. Human diseases with Mendelian inheritance, direct DNA diagnostics. 7. Non-direct DNA diagnostics. 8. RNA diagnostics. 9. New molecular methods in human genetics. 10. New trends in prenetal diagnosis - non-invasive approach. 11. Genetic counselling in reproduction genetics, genetic cause of infertility, prenatal and preimplantation genetic diagnosis. 12. Modern whole-genome methods in preimplantation genetic diagnosis. 13. Human metabollic defects. 14. Personal identification (paternity, forensics).
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- The course is taught annually.
The course is taught: every week. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
Bi7250 Medical genetics and genetic counseling
Faculty of ScienceSpring 2024
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer)
doc. RNDr. Petr Kuglík, CSc. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Mon 19. 2. to Sun 26. 5. Tue 16:00–17:50 B11/305
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 12 fields of study the course is directly associated with, display
- Course objectives
- The aim of this course is to provide a basic insight into human genetics and to familiarise students with basic principles and methods of medical genetics.
- Learning outcomes
- At the end of the course, students should be able to understand the principles of medical genetics; to describe and explain methods used in medical genetics; to apply learned knowledge for solving model examples in clinical medicine.
- Syllabus
- 1. Medical genetics and genetic counselling. 2. Etics and law in medical genetics. 3. Rare diseases. 4. Preventive approach in medical genetics, primary and secondary prevention. 5. New approaches in human cytogenetics. Genetics of disorders of intellectual development. 6. Human diseases with Mendelian inheritance, direct DNA diagnostics. 7. Non-direct DNA diagnostics. 8. RNA diagnostics. 9. New molecular methods in human genetics. 10. New trends in prenetal diagnosis - non-invasive approach. 11. Genetic counselling in reproduction genetics, genetic cause of infertility, prenatal and preimplantation genetic diagnosis. 12. Modern whole-genome methods in preimplantation genetic diagnosis. 13. Human metabollic defects. 14. Personal identification (paternity, forensics).
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
Bi7250 Medical genetics and genetic counseling
Faculty of ScienceSpring 2023
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer)
doc. RNDr. Petr Kuglík, CSc. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Tue 16:00–17:50 B11/305
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 12 fields of study the course is directly associated with, display
- Course objectives
- The aim of this course is to provide a basic insight into human genetics and to familiarise students with basic principles and methods of medical genetics.
- Learning outcomes
- At the end of the course, students should be able to understand the principles of medical genetics; to describe and explain methods used in medical genetics; to apply learned knowledge for solving model examples in clinical medicine.
- Syllabus
- 1. Medical genetics and genetic counselling. 2. Etics and law in medical genetics. 3. Rare diseases. 4. Preventive approach in medical genetics, primary and secondary prevention. 5. New approaches in human cytogenetics. Genetics of disorders of intellectual development. 6. Human diseases with Mendelian inheritance, direct DNA diagnostics. 7. Non-direct DNA diagnostics. 8. RNA diagnostics. 9. New molecular methods in human genetics. 10. New trends in prenetal diagnosis - non-invasive approach. 11. Genetic counselling in reproduction genetics, genetic cause of infertility, prenatal and preimplantation genetic diagnosis. 12. Modern whole-genome methods in preimplantation genetic diagnosis. 13. Human metabollic defects. 14. Personal identification (paternity, forensics).
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
Bi7250 Medical genetics and genetic counseling
Faculty of ScienceSpring 2022
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer)
doc. RNDr. Petr Kuglík, CSc. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Tue 16:00–17:50 B11/305
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 12 fields of study the course is directly associated with, display
- Course objectives
- The aim of this course is to provide a basic insight into human genetics and to familiarise students with basic principles and methods of medical genetics.
- Learning outcomes
- At the end of the course, students should be able to understand the principles of medical genetics; to describe and explain methods used in medical genetics; to apply learned knowledge for solving model examples in clinical medicine.
- Syllabus
- 1. Medical genetics and genetic counselling. 2. Etics and law in medical genetics. 3. Rare diseases. 4. Preventive approach in medical genetics, primary and secondary prevention. 5. New approaches in human cytogenetics. Genetics of disorders of intellectual development. 6. Human diseases with Mendelian inheritance, direct DNA diagnostics. 7. Non-direct DNA diagnostics. 8. RNA diagnostics. 9. New molecular methods in human genetics. 10. New trends in prenetal diagnosis - non-invasive approach. 11. Genetic counselling in reproduction genetics, genetic cause of infertility, prenatal and preimplantation genetic diagnosis. 12. Modern whole-genome methods in preimplantation genetic diagnosis. 13. Human metabollic defects. 14. Personal identification (paternity, forensics).
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
Bi7250 Medical genetics and genetic counseling
Faculty of ScienceSpring 2021
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer)
doc. RNDr. Petr Kuglík, CSc. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Mon 1. 3. to Fri 14. 5. Tue 15:00–16:50 online_B4
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 12 fields of study the course is directly associated with, display
- Course objectives
- The aim of this course is to provide a basic insight into human genetics and to familiarise students with basic principles and methods of medical genetics.
- Learning outcomes
- At the end of the course, students should be able to understand the principles of medical genetics; to describe and explain methods used in medical genetics; to apply learned knowledge for solving model examples in clinical medicine.
- Syllabus
- 1. Medical genetics and genetic counselling. 2. Etics and law in medical genetics. 3. Rare diseases. 4. Preventive approach in medical genetics, primary and secondary prevention. 5. New approaches in human cytogenetics. Genetics of disorders of intellectual development. 6. Human diseases with Mendelian inheritance, direct DNA diagnostics. 7. Non-direct DNA diagnostics. 8. RNA diagnostics. 9. New molecular methods in human genetics. 10. New trends in prenetal diagnosis - non-invasive approach. 11. Genetic counselling in reproduction genetics, genetic cause of infertility, prenatal and preimplantation genetic diagnosis. 12. Modern whole-genome methods in preimplantation genetic diagnosis. 13. Human metabollic defects. 14. Personal identification (paternity, forensics).
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
Bi7250 Medical genetics and genetic counseling
Faculty of ScienceSpring 2020
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer)
doc. RNDr. Petr Kuglík, CSc. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Tue 15:00–16:50 B11/306
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 12 fields of study the course is directly associated with, display
- Course objectives
- The aim of this course is to provide a basic insight into human genetics and to familiarise students with basic principles and methods of medical genetics.
- Learning outcomes
- At the end of the course, students should be able to understand the principles of medical genetics; to describe and explain methods used in medical genetics; to apply learned knowledge for solving model examples in clinical medicine.
- Syllabus
- 1. Medical genetics and genetic counselling. 2. Etics and law in medical genetics. 3. Rare diseases. 4. Preventive approach in medical genetics, primary and secondary prevention. 5. New approaches in human cytogenetics. Genetics of disorders of intellectual development. 6. Human diseases with Mendelian inheritance, direct DNA diagnostics. 7. Non-direct DNA diagnostics. 8. RNA diagnostics. 9. New molecular methods in human genetics. 10. New trends in prenetal diagnosis - non-invasive approach. 11. Genetic counselling in reproduction genetics, genetic cause of infertility, prenatal and preimplantation genetic diagnosis. 12. Modern whole-genome methods in preimplantation genetic diagnosis. 13. Human metabollic defects. 14. Personal identification (paternity, forensics).
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
Bi7250 Medical genetics and genetic counseling
Faculty of ScienceSpring 2019
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
doc. RNDr. Petr Kuglík, CSc. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Mon 18. 2. to Fri 17. 5. Tue 15:00–16:50 B11/306
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics ) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and acquired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invasive and Noninvasive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Diseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further comments (probably available only in Czech)
- Study Materials
The course is taught annually.
General note: Další přednášející: doc. MUDr. Dalibor Valík, Ph.D., DABCC. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Medical genetics and genetic counseling
Faculty of Sciencespring 2018
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
doc. RNDr. Petr Kuglík, CSc. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Tue 15:00–16:50 B11/306
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and acquired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invasive and Noninvasive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Diseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- written exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Medical genetics and genetic counseling
Faculty of ScienceSpring 2017
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
doc. RNDr. Petr Kuglík, CSc. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Mon 20. 2. to Mon 22. 5. Tue 15:00–16:50 B11/235
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and acquired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invasive and Noninvasive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Diseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Medical genetics and genetic counseling
Faculty of ScienceSpring 2016
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
doc. RNDr. Petr Kuglík, CSc. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Tue 15:00–16:50 B11/235
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and acquired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invasive and Noninvasive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Diseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- written exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2015
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Tue 15:00–16:50 B11/235
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 6 fields of study the course is directly associated with, display
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and acquired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invasive and Noninvasive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Diseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2014
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Tue 15:00–16:50 B11/235
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- Anthropology (programme PřF, M-BI)
- Cellular and Molecular Diagnostics (programme PřF, B-BI)
- Molecular Biology and Genetics (programme PřF, N-BI)
- Molecular Biology and Genetics (programme PřF, N-EXB)
- Molecular Biology and Genetics (programme PřF, N-EXB, specialization Antropogenetika)
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and acquired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invasive and Noninvasive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Diseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2013
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Tue 15:00–16:50 B11/235
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- Anthropology (programme PřF, M-BI)
- Cellular and Molecular Diagnostics (programme PřF, B-BI)
- Molecular Biology and Genetics (programme PřF, N-BI)
- Molecular Biology and Genetics (programme PřF, N-EXB)
- Molecular Biology and Genetics (programme PřF, N-EXB, specialization Antropogenetika)
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine. .
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2012
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Timetable
- Tue 16:00–17:50 B11/235
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- Anthropology (programme PřF, M-BI)
- Anthropology (programme PřF, N-BC)
- Cellular and Molecular Diagnostics (programme PřF, B-BI)
- Molecular Biology and Genetics (programme PřF, N-BI)
- Molecular Biology and Genetics (programme PřF, N-EXB)
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine. .
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2011
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Vladimíra Vallová, Ph.D. (lecturer)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Jitka Kadlecová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: RNDr. Vladimíra Vallová, Ph.D. - Timetable
- Thu 15:00–16:50 KDIN N01062
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- Anthropology (programme PřF, M-BI)
- Anthropology (programme PřF, N-BC)
- Cellular and Molecular Diagnostics (programme PřF, B-BI)
- Molecular Biology and Genetics (programme PřF, N-BI)
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine. .
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- The course is taught annually.
- Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2010
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Alexandra Oltová (lecturer), doc. RNDr. Petr Kuglík, CSc. (deputy)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Jitka Kadlecová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc. - Timetable
- Thu 14:00–15:50 KDIN N01062
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine. .
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2009
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Alexandra Oltová (lecturer), doc. RNDr. Petr Kuglík, CSc. (deputy)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Jitka Kadlecová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc. - Timetable
- Thu 15:00–16:50 KDIN N01062
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- The aim of this course is to explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine. The main objectives of the course are the following: Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Assessment methods
- written tests
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2008
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Alexandra Oltová (lecturer), doc. RNDr. Petr Kuglík, CSc. (deputy)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Jitka Kadlecová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc. - Timetable
- Thu 15:00–16:50 KDIN N01062
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- The course is taught annually.
- Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2007
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Alexandra Oltová (lecturer), doc. RNDr. Petr Kuglík, CSc. (deputy)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Jitka Kadlecová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc. - Timetable
- Thu 15:00–16:50 BR1
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2006
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Alexandra Oltová (lecturer), doc. RNDr. Petr Kuglík, CSc. (deputy)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Jitka Kadlecová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc. - Timetable
- Thu 15:00–16:50 BR2
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2005
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Alexandra Oltová (lecturer), doc. RNDr. Petr Kuglík, CSc. (deputy)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Jitka Kadlecová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc. - Timetable
- Thu 16:00–17:50 B1,01004
- Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2004
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Alexandra Oltová (lecturer)
MUDr. Renata Gaillyová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc. - Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- Study Materials
The course is taught annually.
The course is taught: every week. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceAutumn 2002
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Alexandra Oltová (lecturer)
MUDr. Renata Gaillyová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc. - Prerequisites (in Czech)
- SOUHLAS || Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 10 fields of study the course is directly associated with, display
- Course objectives
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- The course is taught annually.
The course is taught: every week. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
Bi7250 Human genetics
Faculty of Sciencespring 2012 - acreditation
The information about the term spring 2012 - acreditation is not made public
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Iveta Valášková, Ph.D. (lecturer)
RNDr. Vladimíra Vallová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc.
Supplier department: Department of Experimental Biology – Biology Section – Faculty of Science - Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Basic genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- Anthropology (programme PřF, M-BI)
- Anthropology (programme PřF, N-BC)
- Cellular and Molecular Diagnostics (programme PřF, B-BI)
- Molecular Biology and Genetics (programme PřF, N-BI)
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine. .
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- The course is taught annually.
The course is taught: every week. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2011 - only for the accreditation
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Alexandra Oltová (lecturer), doc. RNDr. Petr Kuglík, CSc. (deputy)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Jitka Kadlecová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc. - Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- At the end of course students should be able: to understand the principles of medical genetics, to describe and explain the technology and applications of clinical genetics, cytogenetics and molecular genetics in clinical medicine. .
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- SNUSTAD, D. Peter, Michael J. SIMMONS, Jiřina RELICHOVÁ, Jiří DOŠKAŘ, Jiří FAJKUS, Petr HOŘÍN, Aleš KNOLL, Petr KUGLÍK, Jan ŠMARDA, Jana ŠMARDOVÁ, Renata VESELSKÁ and Boris VYSKOT. Genetika (Principles of Genetics). 1st ed. Brno: Masarykova univerzita, 2009, 894 pp. Učebnice. ISBN 978-80-210-4852-2. URL info
- NUSSBAUM, Robert L., Roderick R. MCINNES, Huntington F. WILLARD, James THOMPSON and Margaret Wilson THOMPSON. Klinická genetika : Thompson & Thompson. Translated by Petr Goetz. Vyd. 1. Praha: Triton, 2004, 426, lix. ISBN 8072544756. info
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Teaching methods
- lectures
- Assessment methods
- oral exam
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- The course is taught annually.
The course is taught: every week. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
Bi7250 Human genetics
Faculty of ScienceSpring 2008 - for the purpose of the accreditation
- Extent and Intensity
- 2/0/0. 2 credit(s) (fasci plus compl plus > 4). Type of Completion: zk (examination).
- Teacher(s)
- RNDr. Alexandra Oltová (lecturer), doc. RNDr. Petr Kuglík, CSc. (deputy)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Jitka Kadlecová, Ph.D. (lecturer) - Guaranteed by
- doc. RNDr. Petr Kuglík, CSc.
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: doc. RNDr. Petr Kuglík, CSc. - Prerequisites (in Czech)
- ( Ex_3162 Obecná genetika || Imp_9126 Obecná genetika || B1900 Basic genetics || BMB32 Basic genetics || B6730 Genetics || B8470 Genetics || B3060 Basic genetics || Bi3060 Basic genetics ) && ( Ex_3065 Molekulární biologie || Imp_9115 Molekulární biologie || B3120 Molecular and cell biology || B4030 Molecular biology || B5740 Molecular biology || B6130 Molecular biology || B7940 Molecular biology || B4020 Molecular biology || Bi4020 Molecular biology ) && ( Ex_2315 Cytogenetika || BMB41 Cytogenetics || B6270 Cytogenetics || Bi6270 Cytogenetics || NOW( Bi6270 Cytogenetics )) && ! B7250 Human genetics
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- there are 7 fields of study the course is directly associated with, display
- Course objectives
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Syllabus
- Clinical Cytogenetics, Abnormal Chromosome Constitutions in Humans (numerically and structurally, inborn and equired), Frequency in Human Population and Spontaneous Abortions, Indications for Karyotyping, Prenatal Diagnosis, Invazive and Noninvazive Methods and Indications for Fetal Karyotyping, Detection of Fetal Cells in Maternal Blood, Preimplantation Diagnosis. Molecular clinic genetics: Human genome, human disease genes, mutation and polymorphisms of human DNA, molecular biology methods in diagnostics of pathologic genes (isolation of DNA and RNA, restriction analyses, DNA hybridization assays, PCR - based DNA analyses, electrophoretic methods, screening of mutations, single strand conformation polymorphism), Prenatal and postnatal DNA based diagnosis of common single gene defects (Cystic fibrosis, Huntington disease, Fragile X syndrome, Duchenne muscular dystrophy, Hemophilia A), cardiac defects, personal identification (paternity, forensics). Clinical Genetics, Genetic Deseases, Clinical features, Prenatal and Postnatal Diagnosis of Inborn Chromosomal Aberrations and Genetic Consulting, Prognosis, Ethics in Clinical Genetics.
- Literature
- HATINA, Jiří and Brian D. SYKES. Lékařská genetika : problémy a přístupy. Vyd. 1. Praha: Academia, 1999, 296 s. ISBN 8020007008. info
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- The course is taught annually.
The course is taught: every week. - Listed among pre-requisites of other courses
- Bi7250c Medical genetics and genetical consulting - practice
Bi0422 && Bi0311 && (NOW(Bi7250) || Bi7250) - Bi7290 Human Genetics and Genomics Seminar
Bi7250 || NOW(Bi7250) - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250c Medical genetics and genetical consulting - practice
- Teacher's information
- http://orion.sci.muni.cz/kgmb/student/7250/Sylabus2004.htm
- Enrolment Statistics (recent)