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Australian and New Zealand Journal of Ophthalmology|December 8, 1998
Treatment of pigment epithelial detachments due to age-related macular degeneration with intra-ocular C3F8 injectionM Gross-Jendroska, C J Flaxel, S D Schwartz, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|February 7, 2001
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1S M Downes, G E Holder, F W Fitzke, et al.Transactions of the Ophthalmological Societies of the United Kingdom|January 1, 1983
DNA probes in X-linked retinitis pigmentosaA F Wright, S Bhattacharya, W H Price, et al.Human Genetics|October 1, 1986
Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimationJ F Clayton, A F Wright, M Jay, et al.The British Journal of Ophthalmology|September 1, 1995
Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19qK Evans, M al-Maghtheh, F W Fitzke, et al.Journal of Medical Genetics|February 25, 1998
A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneityC F Inglehearn, E E Tarttelin, C Plant, et al.Genome Research|February 1, 1996
Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypesS D Wijesuriya, K Evans, M R Jay, et al.Human Genetics|September 10, 1999
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locusI Zito, D L Thiselton, M B Gorin, et al.The British Journal of Ophthalmology|August 1, 1993
Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic studyA T Moore, F Fitzke, M Jay, et al.Human Molecular Genetics|February 1, 1994
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19M al-Maghtheh, C F Inglehearn, T J Keen, et al.Pageof 33