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Gavin Chapman is a Conjoint Senior Lecturer in the School of Clinical Medicine at the University of New South Wales. His research focuses on human genomics, particularly identifying genes that are mutated and cause congenital birth defects, including congenital heart disease. He employs a variety of methodologies, including cell culture and mouse and yeast genetics, to confirm altered functions associated with mutated genes. His studies utilize advanced microscopy techniques to explore and identify developmental defects within mouse models mimicking human congenital diseases. His work is aimed at advancing our understanding of genetic contributions to these health issues.
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