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T P Dryja

Showing results (101-110 of 141) with videos related to

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Investigative Ophthalmology & Visual Science|August 31, 2001
Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degenerationC E Briggs, D Rucinski, P J Rosenfeld, et al.
Nature Genetics|July 3, 1999
Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosaE A Pierce, T Quinn, T Meehan, et al.
Nature Genetics|December 1, 1995
Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesteraseS H Huang, S J Pittler, X Huang, et al.
Genomics|January 1, 1995
Mapping of the human cone transducin alpha-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt diseaseI Magovcevic, S Weremowicz, C C Morton, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 31, 1998
Rod and cone function in the Nougaret form of stationary night blindnessM A Sandberg, B S Pawlyk, J Dan, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosisH Morimura, G A Fishman, S A Grover, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual functionD Sharon, G A Bruns, T L McGee, et al.
Human Mutation|December 19, 2001
Novel frameshift mutations in CRX associated with Leber congenital amaurosisC Rivolta, N E Peck, A B Fulton, et al.
American Journal of Ophthalmology|March 10, 2001
Two families from New England with usher syndrome type IC with distinct haplotypesM M DeAngelis, T L McGee, B J Keats, et al.
The New England Journal of Medicine|March 1, 1984
Homozygosity of chromosome 13 in retinoblastomaT P Dryja, W Cavenee, R White, et al.
Pageof 15

Showing results (101-110 of 141) with videos related to

Sort By:
Pageof 15
Investigative Ophthalmology & Visual Science|August 31, 2001
Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degenerationC E Briggs, D Rucinski, P J Rosenfeld, et al.
Nature Genetics|July 3, 1999
Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosaE A Pierce, T Quinn, T Meehan, et al.
Nature Genetics|December 1, 1995
Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesteraseS H Huang, S J Pittler, X Huang, et al.
Genomics|January 1, 1995
Mapping of the human cone transducin alpha-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt diseaseI Magovcevic, S Weremowicz, C C Morton, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 31, 1998
Rod and cone function in the Nougaret form of stationary night blindnessM A Sandberg, B S Pawlyk, J Dan, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosisH Morimura, G A Fishman, S A Grover, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual functionD Sharon, G A Bruns, T L McGee, et al.
Human Mutation|December 19, 2001
Novel frameshift mutations in CRX associated with Leber congenital amaurosisC Rivolta, N E Peck, A B Fulton, et al.
American Journal of Ophthalmology|March 10, 2001
Two families from New England with usher syndrome type IC with distinct haplotypesM M DeAngelis, T L McGee, B J Keats, et al.
The New England Journal of Medicine|March 1, 1984
Homozygosity of chromosome 13 in retinoblastomaT P Dryja, W Cavenee, R White, et al.
Pageof 15