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V C Sheffield

Showing results (11-20 of 153) with videos related to

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Human Molecular Genetics|October 24, 2001
Molecular genetics of age-related macular degenerationE M Stone, V C Sheffield, G S Hageman
American Journal of Medical Genetics|November 6, 1995
Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome lociR Carmi, K Elbedour, E M Stone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1994
The relationship between granular, lattice type 1, and Avellino corneal dystrophies. A histopathologic studyR Folberg, E M Stone, V C Sheffield, et al.
American Journal of Ophthalmology|January 1, 1995
Retinitis pigmentosa associated with a dominant mutation in codon 46 of the peripherin/RDS gene (arginine-46-stop)B L Lam, K Vandenburgh, V C Sheffield, et al.
Genes, Chromosomes & Cancer|March 1, 1995
Deletion of chromosome arm 17p DNA sequences in pediatric high-grade and juvenile pilocytic astrocytomasJ R Willert, L Daneshvar, V C Sheffield, et al.
Human Molecular Genetics|March 1, 1995
Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genomeJ Dubovsky, V C Sheffield, G M Duyk, et al.
Biotechniques|March 1, 1992
A simple and efficient method for attachment of a 40-base pair, GC-rich sequence to PCR-amplified DNAV C Sheffield, J S Beck, E M Stone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1992
Ocular findings associated with a rhodopsin gene codon 106 mutation. Glycine-to-arginine change in autosomal dominant retinitis pigmentosaG A Fishman, E M Stone, L D Gilbert, et al.
American Journal of Human Genetics|October 30, 1998
A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mappingN B Haider, R Carmi, H Shalev, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989
Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changesV C Sheffield, D R Cox, L S Lerman, et al.
Pageof 16

Showing results (11-20 of 153) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|October 24, 2001
Molecular genetics of age-related macular degenerationE M Stone, V C Sheffield, G S Hageman
American Journal of Medical Genetics|November 6, 1995
Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome lociR Carmi, K Elbedour, E M Stone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1994
The relationship between granular, lattice type 1, and Avellino corneal dystrophies. A histopathologic studyR Folberg, E M Stone, V C Sheffield, et al.
American Journal of Ophthalmology|January 1, 1995
Retinitis pigmentosa associated with a dominant mutation in codon 46 of the peripherin/RDS gene (arginine-46-stop)B L Lam, K Vandenburgh, V C Sheffield, et al.
Genes, Chromosomes & Cancer|March 1, 1995
Deletion of chromosome arm 17p DNA sequences in pediatric high-grade and juvenile pilocytic astrocytomasJ R Willert, L Daneshvar, V C Sheffield, et al.
Human Molecular Genetics|March 1, 1995
Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genomeJ Dubovsky, V C Sheffield, G M Duyk, et al.
Biotechniques|March 1, 1992
A simple and efficient method for attachment of a 40-base pair, GC-rich sequence to PCR-amplified DNAV C Sheffield, J S Beck, E M Stone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1992
Ocular findings associated with a rhodopsin gene codon 106 mutation. Glycine-to-arginine change in autosomal dominant retinitis pigmentosaG A Fishman, E M Stone, L D Gilbert, et al.
American Journal of Human Genetics|October 30, 1998
A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mappingN B Haider, R Carmi, H Shalev, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989
Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changesV C Sheffield, D R Cox, L S Lerman, et al.
Pageof 16