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Genomics|September 1, 1992
Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: further locus heterogeneity in adRPR Bashir, C F Inglehearn, T J Keen, et al.The British Journal of Ophthalmology|November 12, 2003
Genotype-phenotype correlation in British families with X linked congenital stationary night blindnessL E Allen, I Zito, K Bradshaw, et al.American Journal of Human Genetics|September 1, 1990
Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneityD H Lester, C F Inglehearn, R Bashir, et al.Ophthalmology|January 1, 1997
Ocular ultrasound in Alagille syndrome: a new signK K Nischal, M Hingorani, C R Bentley, et al.Genomics|January 1, 1990
No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneityC F Inglehearn, M Jay, D H Lester, et al.Nature Genetics|May 1, 1993
A new locus for autosomal dominant retinitis pigmentosa on chromosome 7pC F Inglehearn, S A Carter, T J Keen, et al.Human Molecular Genetics|June 9, 1998
Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophyR E Kelsell, K Gregory-Evans, A M Payne, et al.Transactions of the Ophthalmological Societies of the United Kingdom|January 1, 1985
Autoimmune mechanisms in inflammatory eye diseaseD C Dumonde, E Kasp-Grochowska, J P Banga, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 2002
Visual outcomes in the subfoveal radiotherapy study: a randomized controlled trial of teletherapy for age-related macular degenerationP M Hart, U Chakravarthy, G Mackenzie, et al.The British Journal of Ophthalmology|November 21, 2007
ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathyM Michaelides, L L Chen, M A Brantley, et al.Pageof 33