B7250 Human genetics

Faculty of Science
Autumn 2001
Extent and Intensity
2/0/0. 3 credit(s). Type of Completion: zk (examination).
Teacher(s)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
MUDr. Věra Hořínová (lecturer)
RNDr. Alexandra Oltová (lecturer)
RNDr. Marie Vojtíšková, CSc. (lecturer)
Guaranteed by
RNDr. Alexandra Oltová
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: RNDr. Alexandra Oltová
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
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.
Language of instruction
Czech
Further Comments
The course can also be completed outside the examination period.
The course is taught annually.
The course is taught: every week.
Listed among pre-requisites of other courses
The course is also listed under the following terms Autumn 1999, Autumn 2000.

B7250 Human genetics

Faculty of Science
Autumn 2000
Extent and Intensity
2/0/0. 3 credit(s). Type of Completion: zk (examination).
Teacher(s)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Alexandra Oltová (lecturer)
RNDr. Marie Vojtíšková, CSc. (lecturer)
Guaranteed by
RNDr. Alexandra Oltová
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: RNDr. Alexandra Oltová
Prerequisites (in Czech)
B3060 Basic genetics && ( B4020 Molecular biology || B4030 Molecular biology ) && B6270 Cytogenetics && ( B6390 Molecular Methods || B6400 Methods of molecular biology )
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.
Language of instruction
Czech
Further Comments
The course can also be completed outside the examination period.
The course is taught annually.
The course is taught: every week.
Listed among pre-requisites of other courses
The course is also listed under the following terms Autumn 1999, Autumn 2001.

B7250 Human genetics

Faculty of Science
Autumn 1999
Extent and Intensity
2/0/0. 2 credit(s). Type of Completion: zk (examination).
Teacher(s)
MUDr. Renata Gaillyová, Ph.D. (lecturer)
RNDr. Alexandra Oltová (lecturer)
RNDr. Marie Vojtíšková, CSc. (lecturer)
Guaranteed by
RNDr. Alexandra Oltová
Department of Experimental Biology – Biology Section – Faculty of Science
Contact Person: RNDr. Alexandra Oltová
Prerequisites (in Czech)
B3060 Basic genetics && ( B4020 Molecular biology || B4030 Molecular biology || B6130 Molecular biology || B5740 Molecular biology ) && B6270 Cytogenetics
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
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.
Language of instruction
Czech
Further Comments
The course is taught annually.
The course is taught: every week.
Listed among pre-requisites of other courses
The course is also listed under the following terms Autumn 2000, Autumn 2001.
  • Enrolment Statistics (recent)