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S G Jacobson

Showing results (91-100 of 139) with videos related to

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American Journal of Human Genetics|October 27, 1997
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, 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.
Ophthalmology|February 1, 1995
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degenerationM B Gorin, K E Jackson, R E Ferrell, et al.
American Journal of Human Genetics|March 3, 1999
Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosaA J Mears, L Gieser, D Yan, et al.
Investigative Ophthalmology & Visual Science|October 23, 1997
Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR geneS G Jacobson, M Buraczynska, A H Milam, et al.
American Journal of Human Genetics|October 30, 1998
A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27L Gieser, R Fujita, H H Göring, et al.
Investigative Ophthalmology & Visual Science|January 14, 2000
Psychophysical evidence for rod vulnerability in age-related macular degenerationC Owsley, G R Jackson, A V Cideciyan, et al.
American Journal of Human Genetics|August 1, 1995
Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21Y Y Shugart, P Banerjee, J A Knowles, et al.
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|November 4, 2000
A homozygous deletion in RPE65 in a small Sardinian family with autosomal recessive retinal dystrophyW J Poehner, M Fossarello, A L Rapoport, et al.
Pageof 14

Showing results (91-100 of 139) with videos related to

Sort By:
Pageof 14
American Journal of Human Genetics|October 27, 1997
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, 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.
Ophthalmology|February 1, 1995
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degenerationM B Gorin, K E Jackson, R E Ferrell, et al.
American Journal of Human Genetics|March 3, 1999
Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosaA J Mears, L Gieser, D Yan, et al.
Investigative Ophthalmology & Visual Science|October 23, 1997
Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR geneS G Jacobson, M Buraczynska, A H Milam, et al.
American Journal of Human Genetics|October 30, 1998
A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27L Gieser, R Fujita, H H Göring, et al.
Investigative Ophthalmology & Visual Science|January 14, 2000
Psychophysical evidence for rod vulnerability in age-related macular degenerationC Owsley, G R Jackson, A V Cideciyan, et al.
American Journal of Human Genetics|August 1, 1995
Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21Y Y Shugart, P Banerjee, J A Knowles, et al.
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|November 4, 2000
A homozygous deletion in RPE65 in a small Sardinian family with autosomal recessive retinal dystrophyW J Poehner, M Fossarello, A L Rapoport, et al.
Pageof 14