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Ophthalmic Genetics|December 15, 2005
The relative contribution of the X chromosome to ocular phenotypesA W Hewitt, K P BurdonEye (London, England)|February 28, 2009
Mortality in primary open-angle glaucoma: 'two cupped discs and a funeral'A W Hewitt, P Sanfilippo, M A Ring, et al.Journal of Medical Genetics|September 6, 2005
Lack of association of p53 polymorphisms and haplotypes in high and normal tension open angle glaucomaD P Dimasi, A W Hewitt, C M Green, et al.The British Journal of Ophthalmology|February 27, 2009
Advances in telemetric continuous intraocular pressure assessmentT Kakaday, A W Hewitt, N H Voelcker, et al.Eye (London, England)|April 16, 2011
Distribution of conjunctival ultraviolet autofluorescence in a population-based study: the Norfolk Island Eye StudyJ C Sherwin, A W Hewitt, L S Kearns, et al.The British Journal of Ophthalmology|August 4, 2006
The role of the Met98Lys optineurin variant in inherited optic nerve diseasesJ E Craig, A W Hewitt, D P Dimasi, et al.The British Journal of Ophthalmology|July 26, 2008
The natural history of OPA1-related autosomal dominant optic atrophyA C Cohn, C Toomes, A W Hewitt, et al.Genes and Immunity|May 17, 2014
Utility of temporal artery biopsy samples for genome-wide analysis of giant cell arteritisK Cremin, P Leo, J E Harris, et al.Clinical Genetics|August 28, 2007
Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucomaD P Dimasi, A W Hewitt, T Straga, et al.Eye (London, England)|November 27, 2010
Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutationsA C Cohn, C Turnbull, J B Ruddle, et al.Pageof 2