DSpace Collection: http://hdl.handle.net/2328/1589 2013-05-23T18:12:48Z Novel causative mutations in patients with Nance-Horan Syndrome and altered localization of the mutant NHS-A protein isoform http://hdl.handle.net/2328/11243 Title: Novel causative mutations in patients with Nance-Horan Syndrome and altered localization of the mutant NHS-A protein isoform Authors: Sharma, Shiwani; Burdon, Kathryn Penelope; Craig, Jamie E; Dave, Alpana; Jamieson, Robyn; Yaron, Yuval; Billson, Frank; Maldergem, Lionel; Lorenz, Birgit; Gecz, Jozef 2008-01-01T00:00:00Z Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract http://hdl.handle.net/2328/11196 Title: Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract Authors: Mackey, David A; Craig, Jamie E; Burdon, Kathryn Penelope; Lachke, Salil A; Hattersely, Kathryn; Laurie, Kate; Maas, Richard L 2008-01-01T00:00:00Z The PITX3 gene in posterior polar congenital cataract in Australia http://hdl.handle.net/2328/11165 Title: The PITX3 gene in posterior polar congenital cataract in Australia Authors: Burdon, Kathryn Penelope; McKay, James D; Wirth, M Gabriela; Ruddle, Jonathan; Russell-Eggit, Isabelle M; Bhatti, Samira; Dimasi, David Paul; Mackey, David A; Craig, Jamie E 2006-01-01T00:00:00Z A novel locus for X-lined congenital cataract on Xq24 http://hdl.handle.net/2328/11161 Title: A novel locus for X-lined congenital cataract on Xq24 Authors: Craig, Jamie E; Friend, K; Gecz, Jozef; Rattray, K M; Troski, Mark; Mackey, David A; Burdon, Kathryn Penelope 2008-01-01T00:00:00Z