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B Gorin

Showing results (101-110 of 175) with videos related to

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Molecular Vision|November 17, 1999
The genetics of age-related macular degenerationM B Gorin, J C Breitner, P T De Jong, et al.
European Journal of Human Genetics : EJHG|January 5, 2017
Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophyXiaodong Jiao, Anren Li, Zi-Bing Jin, et al.
Clinical Kidney Journal|February 13, 2019
Three patients with injection of intravitreal vascular endothelial growth factor inhibitors and subsequent exacerbation of chronic proteinuria and hypertensionRamy M Hanna, Eduardo A Lopez, Huma Hasnain, et al.
JAMA|March 4, 1992
Screening for von Hippel-Lindau disease by DNA polymorphism analysisG M Glenn, W M Linehan, S Hosoe, et al.
BMC Medical Genetics|August 7, 2012
Molecular diagnosis of putative Stargardt Disease probands by exome sequencingSamuel P Strom, Yong-Qing Gao, Ariadna Martinez, 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.
Current Eye Research|November 1, 1987
Nucleotide sequence for the cDNA of the bovine beta B2 crystallin and assignment of the orthologous human locus to chromosome 22D Hogg, M B Gorin, C Heinzmann, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 1, 1997
A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36J S Andersen, A M Pralea, E A DelBono, et al.
Human Genetics|June 1, 1991
Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locusG M Glenn, L N Daniel, P Choyke, et al.
Metabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)|January 1, 1992
Ophthalmologic manifestations of type B Niemann-Pick diseasesM R Filling-Katz, J K Fink, M B Gorin, et al.
Pageof 18

Showing results (101-110 of 175) with videos related to

Sort By:
Pageof 18
Molecular Vision|November 17, 1999
The genetics of age-related macular degenerationM B Gorin, J C Breitner, P T De Jong, et al.
European Journal of Human Genetics : EJHG|January 5, 2017
Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophyXiaodong Jiao, Anren Li, Zi-Bing Jin, et al.
Clinical Kidney Journal|February 13, 2019
Three patients with injection of intravitreal vascular endothelial growth factor inhibitors and subsequent exacerbation of chronic proteinuria and hypertensionRamy M Hanna, Eduardo A Lopez, Huma Hasnain, et al.
JAMA|March 4, 1992
Screening for von Hippel-Lindau disease by DNA polymorphism analysisG M Glenn, W M Linehan, S Hosoe, et al.
BMC Medical Genetics|August 7, 2012
Molecular diagnosis of putative Stargardt Disease probands by exome sequencingSamuel P Strom, Yong-Qing Gao, Ariadna Martinez, 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.
Current Eye Research|November 1, 1987
Nucleotide sequence for the cDNA of the bovine beta B2 crystallin and assignment of the orthologous human locus to chromosome 22D Hogg, M B Gorin, C Heinzmann, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 1, 1997
A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36J S Andersen, A M Pralea, E A DelBono, et al.
Human Genetics|June 1, 1991
Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locusG M Glenn, L N Daniel, P Choyke, et al.
Metabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)|January 1, 1992
Ophthalmologic manifestations of type B Niemann-Pick diseasesM R Filling-Katz, J K Fink, M B Gorin, et al.
Pageof 18