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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.Lancet (London, England)|October 9, 1982
Anti-retinal autoimmunity and circulating immune complexes in patients with retinal vasculitisD C Dumonde, E Kasp-Grochowska, E Graham, et al.The British Journal of Ophthalmology|January 20, 1999
Papilloedema, a complication of progressive diaphyseal dysplasia: a series of three case reportsM Wright, N R Miller, R M McFadzean, et al.Ophthalmology|September 1, 1994
Bilateral macular drusen in age-related macular degeneration. Prognosis and risk factorsF G Holz, T J Wolfensberger, B Piguet, et al.American Journal of Human Genetics|October 1, 1987
Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14A F Wright, S S Bhattacharya, J F Clayton, et al.Human Molecular Genetics|July 1, 1996
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16C Y Gregory, K Evans, S D Wijesuriya, et al.Nature Genetics|August 10, 2000
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosaR Vervoort, A Lennon, A C Bird, et al.Ophthalmology|February 10, 1999
Ocular abnormalities in Alagille syndromeM Hingorani, K K Nischal, A Davies, et al.Human Molecular Genetics|March 21, 1998
A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1A M Payne, S M Downes, D A Bessant, 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.Pageof 33