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Browsing by Author Laurie, Kate

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PreviewIssue DateTitleAuthor(s)
2010Aldose reductase gene polymorphisms and diabetic retinopathy susceptibilityThorpe, Stacey; Abhary, Sotoodeh; Burdon, Kathryn Penelope; Laurie, Kate; Landers, John A; Goold, L; Lake, Stewart; Petrovsky, Nikolai; Craig, Jamie
2008Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel lociGiunta, Cecilia; Hewitt, Alex W; Craig, Jamie E; Latimer, Paul; Burdon, Kathryn Penelope; Coster, Douglas John; Charlesworth, Jac C; Mills, Richard Arthur; Laurie, Kate
Mar-2013Identification of a novel oligomerization disrupting mutation in CRYAA associated with congenital cataract in a South Australian familyLaurie, Kate; Dave, Alpana; Straga, Tania; Souzeau, Emmanuelle; Chataway, Timothy Kennion; Sykes, Matthew James; Casey, Theresa; Teo, Theodosia; Pater, John Brian; Craig, Jamie E; Sharma, Shiwani; Burdon, Kathryn Penelope
2008Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataractMackey, David A; Craig, Jamie E; Burdon, Kathryn Penelope; Lachke, Salil A; Hattersely, Kathryn; Laurie, Kate; Maas, Richard L
2010A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian aboriginal family maps to 1p35.3-p36.32Hattersely, Kathryn; Laurie, Kate; Leibelt, J E; Gezc, J; Durkin, Shane; Craig, Jamie; Burdon, Kathryn Penelope
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