This unit extends the student's understanding of the concepts of genetics and molecular biology obtained in CXA171 Cell Biology and Function and CXA262 Cell and Molecular Biochemistry. The unit focuses on medical molecular genetics, providing detailed study of genetic mutations and inheritance patterns of genetic diseases. Laboratory sessions will cover molecular diagnostic techniques.
|Unit name||Human Molecular Biology|
|College/School||College of Health and Medicine
School of Health Sciences
|Coordinator||Doctor Stephen Myers|
|Available as student elective?||Yes|
|Delivered By||University of Tasmania|
|Location||Study period||Attendance options||Available to|
- International students
- Domestic students
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Units are offered in attending mode unless otherwise indicated (that is attendance is required at the campus identified). A unit identified as offered by distance, that is there is no requirement for attendance, is identified with a nominal enrolment campus. A unit offered to both attending students and by distance from the same campus is identified as having both modes of study.
|Study Period||Start date||Census date||WW date||End date|
* The Final WW Date is the final date from which you can withdraw from the unit without academic penalty, however you will still incur a financial liability (see withdrawal dates explained for more information).
Unit census dates currently displaying for 2022 are indicative and subject to change. Finalised census dates for 2022 will be available from the 1st October 2021.
- Analyse and interpret theoretical concepts of complex genetics problems related to human disease.
- Demonstrate self-directed learning by accessing, critically evaluating, and synthesising a scientific review from a wide variety of peer-reviewed scientific information sources.
- Communicate, in oral and written format, fundamental genetics disease processes, diagnostics, and treatments in a manner appropriate for an informed scientific audience.
- Implement molecular diagnostic techniques to critically evaluate, interpret, and describe genetic inheritance patterns and genetic disease processes from experimental results.
|Field of Education||Commencing Student Contribution 1||Grandfathered Student Contribution 1||Approved Pathway Course Student Contribution 2||Domestic Full Fee|
- Available as a Commonwealth Supported Place
- HECS-HELP is available on this unit, depending on your eligibility3
- FEE-HELP is available on this unit, depending on your eligibility4
1 Please refer here more information on student contribution amounts.
2 Information on eligibility and Approved Pathway courses can be found here
3 Please refer here for eligibility for HECS-HELP
4 Please refer here for eligibility for FEE-HELP
Please note: international students should refer to this page to get an indicative course cost.
Tutorial – 1 hour (weekly), self-directed learning activities – 10 hours (weekly). A three-day long practical class (approximately 6 hrs - 8 hrs/day) will be held during Week 13.
|Assessment||Quiz (25%)|Quiz (25%)|Laboratory Notebook and Practical Participation (15%)|Oral Presentation (10%)|Complex disease pathology and diagnostics activity (25%)|
|Timetable||View the lecture timetable | View the full unit timetable|
Required readings will be listed in the unit outline prior to the start of classes.
You don’t need a textbook to pass this unit, but it will certainly help you understand the content in more detail. The following textbook will be used in some of the lectures for CXA300 -
|Links||Booktopia textbook finder|
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