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Investigative Ophthalmology & Visual Science|May 1, 2001
Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX geneR T Tzekov, Y Liu, M M Sohocki, et al.Journal of Pediatric Gastroenterology and Nutrition|January 6, 2001
Impact of early dietary intake and blood lipid composition of long-chain polyunsaturated fatty acids on later visual developmentD R Hoffman, E E Birch, D G Birch, et al.Ophthalmology|July 1, 1990
Vitrectomy in eyes at risk for macular hole formationB F Jost, W L Hutton, D G Fuller, et al.Molecular Vision|March 9, 2000
Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7qS J Bowne, L S Sullivan, L Ding, et al.American Journal of Human Genetics|October 30, 1998
A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27L Gieser, R Fujita, H H Göring, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|May 1, 1997
Light reduction and the electroretinogram of preterm infantsK A Kennedy, M A Ipson, D G Birch, et al.American Journal of Human Genetics|June 13, 1998
Evidence for genetic heterogeneity in X-linked congenital stationary night blindnessK M Boycott, W G Pearce, M A Musarella, et al.Nature Genetics|May 10, 2000
Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesisG Clarke, A F Goldberg, D Vidgen, et al.Proceedings of the National Academy of Sciences of the United States of America|March 8, 2005
Lipofuscin accumulation, abnormal electrophysiology, and photoreceptor degeneration in mutant ELOVL4 transgenic mice: a model for macular degenerationG Karan, C Lillo, Z Yang, et al.Molecular Genetics and Metabolism|June 30, 2000
Prevalence of AIPL1 mutations in inherited retinal degenerative diseaseM M Sohocki, I Perrault, B P Leroy, et al.Pageof 19