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Showing results (121-130 of 153) with videos related to

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Human Molecular Genetics|March 1, 1995
Linkage of posterior polymorphous corneal dystrophy to 20q11E Héon, W D Mathers, W L Alward, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 9, 1999
Short tandem repeat polymorphic markers for the rat genome from marker-selected librariesR Y Walder, M R Garrett, A M McClain, 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.
Nature Genetics|December 17, 1997
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)L A Everett, B Glaser, J C Beck, et al.
Nature Genetics|June 10, 1998
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25D Y Nishimura, R E Swiderski, W L Alward, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Gene|April 18, 2000
Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2D A Scott, S Drury, R A Sundstrom, et al.
The New England Journal of Medicine|April 16, 1998
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)W L Alward, J H Fingert, M A Coote, et al.
Human Molecular Genetics|June 1, 1996
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6M E O'Neill, J Marietta, D Nishimura, et al.
Genomics|February 15, 1996
Development of a screening set for new (CAG/CTG)n dynamic mutationsJ M Gastier, T Brody, J C Pulido, et al.
Pageof 16

Showing results (121-130 of 153) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|March 1, 1995
Linkage of posterior polymorphous corneal dystrophy to 20q11E Héon, W D Mathers, W L Alward, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 9, 1999
Short tandem repeat polymorphic markers for the rat genome from marker-selected librariesR Y Walder, M R Garrett, A M McClain, 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.
Nature Genetics|December 17, 1997
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)L A Everett, B Glaser, J C Beck, et al.
Nature Genetics|June 10, 1998
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25D Y Nishimura, R E Swiderski, W L Alward, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Gene|April 18, 2000
Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2D A Scott, S Drury, R A Sundstrom, et al.
The New England Journal of Medicine|April 16, 1998
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)W L Alward, J H Fingert, M A Coote, et al.
Human Molecular Genetics|June 1, 1996
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6M E O'Neill, J Marietta, D Nishimura, et al.
Genomics|February 15, 1996
Development of a screening set for new (CAG/CTG)n dynamic mutationsJ M Gastier, T Brody, J C Pulido, et al.
Pageof 16