Showing results (161-170 of 178) with videos related to
Sort By:
Pageof 18
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.Investigative Ophthalmology & Visual Science|November 30, 2000
RP1 protein truncating mutations predominate at the RP1 adRP locusA Payne, E Vithana, S Khaliq, et al.Investigative Ophthalmology & Visual Science|December 1, 2001
A novel keratocan mutation causing autosomal recessive cornea planaO J Lehmann, M F El-ashry, N D Ebenezer, et al.American Journal of Human Genetics|September 29, 2000
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucomaO J Lehmann, N D Ebenezer, T Jordan, et al.Journal of Medical Genetics|January 7, 2006
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataractA Arora, P J Minogue, X Liu, et al.Nature Genetics|July 11, 2000
Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapyR R Ali, G M Sarra, C Stephens, et al.American Journal of Human Genetics|August 3, 2001
Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophyS E Wilkie, Y Li, E C Deery, et al.Pageof 18