Showing results (131-140 of 138) with videos related to
Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 138 results.
Genomics|June 22, 1999
Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridizationA I den Hollander, M A van Driel, Y J de Kok, et al.Molecular and Cellular Biology|May 29, 2000
Disruption of the 11-cis-retinol dehydrogenase gene leads to accumulation of cis-retinols and cis-retinyl estersC A Driessen, H J Winkens, K Hoffmann, et al.Human Molecular Genetics|April 18, 1998
Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCRF P Cremers, D J van de Pol, M van Driel, et al.Nature Genetics|November 4, 2000
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat proteinC M Pusch, C Zeitz, O Brandau, et al.American Journal of Human Genetics|March 26, 1999
The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt diseaseA Maugeri, M A van Driel, D J van de Pol, et al.American Journal of Human Genetics|June 5, 2001
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) geneA I den Hollander, J R Heckenlively, L I van den Born, et al.American Journal of Human Genetics|April 29, 1998
Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneityJ Oh, L Ho, S Ala-Mello, et al.Nature Genetics|October 3, 1999
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)A I den Hollander, J B ten Brink, Y J de Kok, et al.Pageof 14