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E M Stone

Showing results (81-90 of 174) with videos related to

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Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|March 11, 2000
The genetic aspects of adult-onset glaucoma: a perspective from the Greater Toronto areaD Williams-Lyn, J Flanagan, Y Buys, et al.
American Journal of Medical Genetics|December 23, 1999
Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21N M Ghiasvand, A B Kanis, C Helms, et al.
Human Molecular Genetics|August 1, 1993
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the foveaB E Nichols, A V Drack, K Vandenburgh, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1992
Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosaG A Fishman, K Vandenburgh, E M Stone, et al.
Molecular Biology of the Cell|September 3, 1999
The conserved core of a human SIR2 homologue functions in yeast silencingJ M Sherman, E M Stone, L L Freeman-Cook, et al.
Ophthalmology|February 1, 1997
Serine-27-phenylalanine mutation within the peripherin/RDS gene in a family with cone dystrophyG A Fishman, E M Stone, K R Alexander, et al.
Survey of Ophthalmology|October 2, 2001
Autosomal dominant Stargardt-like macular dystrophyL A Donoso, A O Edwards, A Frost, et al.
Ophthalmology|September 1, 1990
Autosomal dominant neovascular inflammatory vitreoretinopathyS R Bennett, J C Folk, A E Kimura, et al.
Ophthalmology|April 1, 1993
Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucomaA T Johnson, A V Drack, A E Kwitek, et al.
Human Molecular Genetics|January 1, 1995
Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15R Carmi, T Rokhlina, A E Kwitek-Black, et al.
Pageof 18

Showing results (81-90 of 174) with videos related to

Sort By:
Pageof 18
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|March 11, 2000
The genetic aspects of adult-onset glaucoma: a perspective from the Greater Toronto areaD Williams-Lyn, J Flanagan, Y Buys, et al.
American Journal of Medical Genetics|December 23, 1999
Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21N M Ghiasvand, A B Kanis, C Helms, et al.
Human Molecular Genetics|August 1, 1993
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the foveaB E Nichols, A V Drack, K Vandenburgh, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1992
Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosaG A Fishman, K Vandenburgh, E M Stone, et al.
Molecular Biology of the Cell|September 3, 1999
The conserved core of a human SIR2 homologue functions in yeast silencingJ M Sherman, E M Stone, L L Freeman-Cook, et al.
Ophthalmology|February 1, 1997
Serine-27-phenylalanine mutation within the peripherin/RDS gene in a family with cone dystrophyG A Fishman, E M Stone, K R Alexander, et al.
Survey of Ophthalmology|October 2, 2001
Autosomal dominant Stargardt-like macular dystrophyL A Donoso, A O Edwards, A Frost, et al.
Ophthalmology|September 1, 1990
Autosomal dominant neovascular inflammatory vitreoretinopathyS R Bennett, J C Folk, A E Kimura, et al.
Ophthalmology|April 1, 1993
Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucomaA T Johnson, A V Drack, A E Kwitek, et al.
Human Molecular Genetics|January 1, 1995
Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15R Carmi, T Rokhlina, A E Kwitek-Black, et al.
Pageof 18