units
BMS2042
Faculty of Medicine, Nursing and Health Sciences
This unit entry is for students who completed this unit in 2015 only. For students planning to study the unit, please refer to the unit indexes in the the current edition of the Handbook. If you have any queries contact the managing faculty for your course or area of study.
Refer to the specific census and withdrawal dates for the semester(s) in which this unit is offered.
Level | Undergraduate |
Faculty | Faculty of Medicine, Nursing and Health Sciences |
Organisational Unit | School of Biomedical Sciences |
Offered | Clayton Second semester 2015 (Day) |
Coordinator(s) | Associate Professor Coral Warr |
This unit introduces the basic genetic principles underlying modern human genetics. Topics include the identification, characterisation and mapping of human genes; the value of model organisms; the significance of the Human Genome Project; how genes function and how genetic malfunction can lead to genetic disease; how an understanding of such diseases at the molecular level may assist in diagnosis, prevention and therapy; the roles of gene regulation and mutation in cancer; genetic counselling and ways of calculating risk of recurrence of a genetic disease; ethical issues relevant to human genetics. Practicals include an introduction to molecular and cytogenetic techniques.
Upon successful completion of this unit, students should be able to:
Students will have the background to undertake more advanced studies in genetics at third year level.
Examination (50%)
Continuous assessment (Mini-quizzes, laboratory reports and oral presentation) (35%)
Essay (15%)
A pass in the final exam must be obtained to pass the unit.
3 lectures and 3 hours practical (or equivalent) per week.
See also Unit timetable information
Must be enrolled in one of the following:
+ Bachelor of Biomedical Science (including double degree programs)
+ Bachelor of Biomedical Science (Scholar Program)
+ Bachelor of Biomedical Science Advanced with Honours
+ Bachelor of Biotechnology