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The British Journal of Ophthalmology|January 1, 1995
Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expressionR Y Kim, F W Fitzke, A T Moore, et al.
The British Journal of Ophthalmology|February 22, 2005
A detailed phenotypic study of "cone dystrophy with supernormal rod ERG"M Michaelides, G E Holder, A R Webster, et al.
The British Journal of Ophthalmology|May 29, 2003
Interobserver agreement on visual field progression in glaucoma: a comparison of methodsA C Viswanathan, D P Crabb, A I McNaught, et al.
The British Journal of Ophthalmology|May 1, 1994
Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding siteS L Owens, F W Fitzke, C F Inglehearn, et al.
The British Journal of Ophthalmology|October 27, 2007
Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophyA G Robson, M Michaelides, V A Luong, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
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