Showing results (161-170 of 213) with videos related to

Sort By:
Pageof 22
Plos One|March 22, 2014
Molecular genetics of FAM161A in North American patients with early-onset retinitis pigmentosaGiulia Venturini, Silvio Alessandro Di Gioia, Shyana Harper, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2000
A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3)D H Hong, B S Pawlyk, J Shang, et al.
Investigative Ophthalmology & Visual Science|August 31, 2001
Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degenerationC E Briggs, D Rucinski, P J Rosenfeld, et al.
Nature Genetics|September 23, 2008
Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycleDyonne T Hartong, Mayura Dange, Terri L McGee, et al.
American Journal of Ophthalmology|March 10, 2001
Two families from New England with usher syndrome type IC with distinct haplotypesM M DeAngelis, T L McGee, B J Keats, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 14, 2012
Genotype-phenotype correlations in Bardet-Biedl syndromeAnthony B Daniels, Michael A Sandberg, Jianjun Chen, et al.
Investigative Ophthalmology & Visual Science|August 1, 1992
Plasma docosahexaenoic acid levels in various genetic forms of retinitis pigmentosaJ Gong, B Rosner, D G Rees, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2004
Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone functionKoji M Nishiguchi, James S Friedman, Michael A Sandberg, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual functionD Sharon, G A Bruns, T L McGee, et al.
Pageof 22