T D Bloom|G A Fishman|B S Traubert - JoVE Visualize

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Human Molecular Genetics|February 1, 1994

Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complexA F Roux, J Rommens, C McDowell, et al.

The British Journal of Ophthalmology|May 30, 2002

Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemiaM Flynn Roberts, G A Fishman, D K Roberts, et al.

Ophthalmology|December 17, 1998

X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60G A Fishman, S Grover, S G Jacobson, et al.

Genomics|October 1, 1990

Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa familiesM A Musarella, L Anson-Cartwright, S M Leal, et al.

Ophthalmology|September 15, 1999

Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or olderS Grover, G A Fishman, R J Anderson, et al.

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.

Pageof 21

Showing results (191-200 of 209) with videos related to

Sort By:

Pageof 21

Human Molecular Genetics|February 1, 1994

Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complexA F Roux, J Rommens, C McDowell, et al.

The British Journal of Ophthalmology|May 30, 2002

Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemiaM Flynn Roberts, G A Fishman, D K Roberts, et al.

Ophthalmology|December 17, 1998

X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60G A Fishman, S Grover, S G Jacobson, et al.

Genomics|October 1, 1990

Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa familiesM A Musarella, L Anson-Cartwright, S M Leal, et al.

Ophthalmology|September 15, 1999

Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or olderS Grover, G A Fishman, R J Anderson, et al.

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.

Pageof 21