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Molecular Vision|April 18, 2007
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosaMeredith O Sweeney, Terri L McGee, Eliot L Berson, et al.Molecular Vision|December 15, 2006
A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosaGeetha H Mylvaganam, Terri L McGee, Eliot L Berson, et al.Experimental Eye Research|November 1, 1991
Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesteraseP R Cotran, G A Bruns, E L Berson, et al.Transactions of the Ophthalmological Societies of the United Kingdom|January 1, 1979
Foveal cone electroretinograms in strabismic amblyopia: comparison with juvenile macular degeneration, macular scars, and optic atrophyS G Jacobson, M A Sandberg, M H Effron, et al.Investigative Ophthalmology & Visual Science|March 1, 1988
Rod ERG diurnal rhythm in some patients with dominant retinitis pigmentosaM A Sandberg, C M Baruzzi, A H Hanson, et al.Molecular Vision|February 20, 2003
Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosisCarlo Rivolta, Radha Ayyagari, Paul A Sieving, et al.American Journal of Human Genetics|May 10, 2011
A missense mutation in PRPF6 causes impairment of pre-mRNA splicing and autosomal-dominant retinitis pigmentosaGoranka Tanackovic, Adriana Ransijn, Carmen Ayuso, et al.Investigative Ophthalmology & Visual Science|March 1, 1997
Evaluation of the human gene encoding recoverin in patients with retinitis pigmentosa or an allied diseaseA H Parminder, A Murakami, G Inana, et al.Experimental Eye Research|August 1, 1997
ERG abnormalities in relation to histopathologic findings in vitiligo mutant miceM Tang, B S Pawlyk, B Kosaras, et al.American Journal of Human Genetics|November 5, 1997
Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 alleleT L McGee, M Devoto, J Ott, et al.Pageof 22