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Experimental Eye Research|February 1, 1996
Screening of the PDE6B gene in patients with autosomal dominant retinitis pigmentosaY Q Gao, M Danciger, D Y Zhao, et al.Molecular Vision|September 22, 1998
Exon screening of the genes encoding the beta- and gamma-subunits of cone transducin in patients with inherited retinal diseaseY Q Gao, M Danciger, N B Akhmedov, et al.Clinical Genetics|March 18, 2004
Mutational spectrum in Usher syndrome type IIX M Ouyang, D Yan, J F Hejtmancik, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Rhodopsin mutations in autosomal dominant retinitis pigmentosaC H Sung, C M Davenport, J C Hennessey, et al.American Journal of Human Genetics|July 1, 1993
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsinJ P Macke, C M Davenport, S G Jacobson, et al.Genomics|April 2, 1998
Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3P Banerjee, C A Lewis, P W Kleyn, et al.Genomics|August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11B Wissinger, H Jägle, S Kohl, et al.Experimental Eye Research|February 5, 2002
Concentric retinitis pigmentosa: clinicopathologic correlationsA H Milam, E B De Castro, J E Smith, et al.Clinical Genetics|March 13, 2003
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian alleleX M Ouyang, J F Hejtmancik, S G Jacobson, et al.Investigative Ophthalmology & Visual Science|May 8, 2000
Allelic variation in the VMD2 gene in best disease and age-related macular degenerationA J Lotery, F L Munier, G A Fishman, et al.Pageof 13