Molecular Pathology
Undergraduate
Undergraduate
BIOL 3006
Undergraduate
No
010925
4.5
No
School of Pharmacy and Medical Sciences
This course is designed to provide students with an understanding of the application of biochemical and molecular techniques for the detection, monitoring and assessment of metabolic and genetic diseases.
Role of the clinical chemistry laboratory in diagnosis of diseases. Specimen collection and handling. Quality assurance; sources of error. Use and establishment of reference ranges. Laboratory investigation of disorders of water and electrolyte balance; acid/base balance; kidney function; liver function; carbohydrate metabolism; calcium and phosphate metabolism. Eukaryote genes: structure, function and control; translation control. Genomics. DNA sequence analysis, gene mapping; ethical issues. Diagnostic techniques: nucleic acid amplification, mutation detection, gene expression analysis, chromosome analysis and protein detection. Therapy for genetic diseases.
Bishop ML, Fody EP, Schoeff L. 2013, Clinical Chemistry - Techniques, Principles, Correlations, 7, Lippincott Williams and Wilkins
Read A, Donnai D 2011, New Clinical Genetics, 2nd, Scion
All first and second year courses in the Bachelor of Laboratory Medicine program.
Nil
Component | Duration | ||
---|---|---|---|
INTERNAL, CITY EAST | |||
Lecture | 2 hours x 13 weeks | ||
Tutorial | 1 hour x 13 weeks | ||
Practical | 5 hours x 8 weeks |
Note: These components may or may not be scheduled in every study period. Please refer to the timetable for further details.
Examination, Practical exercises, Test
EFTSL*: 0.125
Commonwealth Supported program (Band 2)
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Fee-paying program for domestic and international students
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Non-award enrolment
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* Equivalent Full Time Study Load. Please note: all EFTSL values are published and calculated at ten decimal places. Values are displayed to three decimal places for ease of interpretation.