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Human Molecular Genetics|March 16, 2004
Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataractM A Reddy, O A Bateman, C Chakarova, et al.Genomics|August 10, 1995
A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7pT J Keen, C F Inglehearn, E D Green, et al.The British Journal of Ophthalmology|June 19, 2003
A clinical, histopathological, and genetic study of Avellino corneal dystrophy in British familiesM F El-Ashry, M M Abd El-Aziz, D F P Larkin, et al.Nature Genetics|October 4, 2000
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28C Alexander, M Votruba, U E Pesch, et al.Human Genetics|September 10, 1999
Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani originV Berry, D Mackay, S Khaliq, et al.The British Journal of Ophthalmology|November 1, 1994
Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosaJ J Wroblewski, J A Wells, A Eckstein, et al.Genomics|December 1, 1991
Genetic and physical mapping around the properdin P geneM P Coleman, J C Murray, H F Willard, et al.Nature|May 17, 1984
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28S S Bhattacharya, A F Wright, J F Clayton, et al.Annals of Human Genetics|May 31, 2008
Large-scale molecular analysis of a 34 Mb interval on chromosome 6q: major refinement of the RP25 intervalM M Abd El-Aziz, I Barragan, C O'Driscoll, et al.Experimental Eye Research|April 20, 2001
Spectrum of mutations in USH2A in British patients with Usher syndrome type IIB P Leroy, J A Aragon-Martin, M D Weston, et al.Pageof 37