PřF:B7250 Human genetics - Course Information
B7250 Human genetics
Faculty of ScienceAutumn 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
- Anthropology (programme PřF, B-BI)
- Anthropology (programme PřF, M-BI)
- Anthropology (programme PřF, N-BI)
- Biophysics (programme PřF, M-FY)
- Cellular and Molecular Diagnostics (programme PřF, B-BI)
- Molecular Biology and Genetics (programme PřF, M-BI)
- Molecular Biology and Genetics (programme PřF, N-BI)
- 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
- Bi7250 Medical genetics and genetic counseling
(Ex_3162 || Imp_9126 || B1900 || BMB32 || B6730 || B8470 || B3060 || Bi3060) && (Ex_3065 || Imp_9115 || B3120 || B4030 || B5740 || B6130 || B7940 || B4020 || Bi4020) && (Ex_2315 || BMB41 || B6270 || Bi6270 || NOW(Bi6270)) && !B7250 - Bi9325 Human Molecular Genetics
(B7250 || Bi7250) && (Bi6401 || Bi3002 || Bi6491 || Bi6005 || Bi6006 || Bi6007 || Bi6122 || souhlas)
- Bi7250 Medical genetics and genetic counseling
- Enrolment Statistics (recent)
- Permalink: https://is.muni.cz/course/sci/autumn2001/B7250