Clinical Genetics Group

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Disease Gene Identification Using High-Throughput Genomic Technologies

Tiffin, Heather Rachel (Thesis, Master of Science, 2012)

Identification of the underlying genetic and molecular components that contribute to human disease can provide significant insight into the biological processes that underlie the development and regulation of affected ...
Investigation of a mutation in CYP26B1

Eerens, Yoska (Thesis, Bachelor of Medical Science with Honours, 2011)

Retinoic acid is known to have several important roles in embryonic development, including limb and hindbrain development and has been shown to induce neural tube defects when it is present at teratogenic levels. The CYP26 ...