Predictive genetic testing in minors for Myocilin juvenile onset open angle glaucoma
Souzeau, E., Glading, J., Ridge, B., Wechsler, D., Chehade, M., Dubowsky, A., Burdon, K.P., Craig, J.E.
Published in Clinical genetics (01.12.2015)
Published in Clinical genetics (01.12.2015)
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Visual outcomes following vitrectomy for diabetic retinopathy amongst Indigenous and non‐Indigenous Australians in South Australia and the Northern Territory
Kaidonis, Georgia, Hassall, Mark M, Phillips, Russell, Raymond, Grant, Saha, Niladri, Wong, George HC, Gilhotra, Jagjit S, Liu, Ebony, Burdon, Kathryn P, Henderson, Tim, Newland, Henry, Lake, Stewart R, Craig, Jamie E
Published in Clinical & experimental ophthalmology (01.05.2018)
Published in Clinical & experimental ophthalmology (01.05.2018)
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Investigation of crystallin genes in familial cataract, and report of two disease associated mutations
Burdon, K P, Wirth, M G, Mackey, D A, Russell-Eggitt, I M, Craig, J E, Elder, J E, Dickinson, J L, Sale, M M
Published in British journal of ophthalmology (01.01.2004)
Published in British journal of ophthalmology (01.01.2004)
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Journal Article
Diabetic retinopathy is not associated with carbonic anhydrase gene polymorphisms
Abhary, S, Burdon, K P, Gupta, A, Petrovsky, N, Craig, J E
Published in Molecular vision (13.06.2009)
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Published in Molecular vision (13.06.2009)
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A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32
Hattersley, Kathryn, Laurie, Kate J, Liebelt, Jan E, Gecz, Jozef, Durkin, Shane R, Craig, Jamie E, Burdon, Kathryn P
Published in BMC genetics (19.11.2010)
Published in BMC genetics (19.11.2010)
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Journal Article
Investigation of crystallin genes in familial cataract, and report of two disease associated mutations
Burdon, K P, Wirth, M G, Mackey, D A, Russell-Eggitt, I M, Craig, J E, Elder, J E, Dickinson, J L, Sale, M M
Published in Journal of medical genetics (01.03.2004)
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Published in Journal of medical genetics (01.03.2004)
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