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G A Fishman

Showing results (211-220 of 224) with videos related to

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Investigative Ophthalmology & Visual Science|October 3, 2001
CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate geneM Danciger, J Hendrickson, J Lyon, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990
Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity testsJ Ott, S Bhattacharya, J D Chen, 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.
Nature Genetics|July 14, 1998
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, 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.
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Human Mutation|May 12, 2009
Predicting the pathogenicity of RPE65 mutationsA R Philp, M Jin, S Li, et al.
Investigative Ophthalmology & Visual Science|June 14, 2000
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosaS G Jacobson, A V Cideciyan, A Iannaccone, et al.
Neuron|January 14, 1998
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degenerationP K Swain, S Chen, Q L Wang, et al.
American Journal of Human Genetics|December 18, 1997
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosaM Buraczynska, W Wu, R Fujita, et al.
Pageof 23

Showing results (211-220 of 224) with videos related to

Sort By:
Pageof 23
Investigative Ophthalmology & Visual Science|October 3, 2001
CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate geneM Danciger, J Hendrickson, J Lyon, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990
Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity testsJ Ott, S Bhattacharya, J D Chen, 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.
Nature Genetics|July 14, 1998
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, 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.
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Human Mutation|May 12, 2009
Predicting the pathogenicity of RPE65 mutationsA R Philp, M Jin, S Li, et al.
Investigative Ophthalmology & Visual Science|June 14, 2000
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosaS G Jacobson, A V Cideciyan, A Iannaccone, et al.
Neuron|January 14, 1998
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degenerationP K Swain, S Chen, Q L Wang, et al.
American Journal of Human Genetics|December 18, 1997
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosaM Buraczynska, W Wu, R Fujita, et al.
Pageof 23