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V C Sheffield

Showing results (41-50 of 153) with videos related to

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Investigative Ophthalmology & Visual Science|July 1, 1996
Photoreceptor function in heterozygotes with insertion or deletion mutations in the RDS geneS G Jacobson, A V Cideciyan, C M Kemp, et al.
Molecular Psychiatry|January 26, 2005
Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flowB-C Ho, T H Wassink, D S O'Leary, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/RDS geneR G Weleber, R E Carr, W H Murphey, et al.
Prenatal Diagnosis|March 22, 2001
Prenatal diagnosis of malignant osteopetrosis in Bedouin families by linkage analysisH Shalev, A Mishori-Dery, J Kapelushnik, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1997
Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)J Brown, J H Fingert, C M Taylor, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1991
Identification of a germ-line mutation in the p53 gene in a patient with an intracranial ependymomaA K Metzger, V C Sheffield, G Duyk, et al.
American Journal of Human Genetics|March 1, 1992
Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesisP H Cogen, L Daneshvar, A K Metzger, et al.
American Journal of Human Genetics|March 1, 1992
Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, J S Beck, B Nichols, et al.
Nucleic Acids Research|February 25, 1982
Construction and partial characterization of two recombinant cDNA clones for procollagen from chicken cartilageE Vuorio, L Sandell, D Kravis, et al.
Ophthalmology|August 1, 1994
Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosaG A Fishman, E Stone, L D Gilbert, et al.
Pageof 16

Showing results (41-50 of 153) with videos related to

Sort By:
Pageof 16
Investigative Ophthalmology & Visual Science|July 1, 1996
Photoreceptor function in heterozygotes with insertion or deletion mutations in the RDS geneS G Jacobson, A V Cideciyan, C M Kemp, et al.
Molecular Psychiatry|January 26, 2005
Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flowB-C Ho, T H Wassink, D S O'Leary, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/RDS geneR G Weleber, R E Carr, W H Murphey, et al.
Prenatal Diagnosis|March 22, 2001
Prenatal diagnosis of malignant osteopetrosis in Bedouin families by linkage analysisH Shalev, A Mishori-Dery, J Kapelushnik, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1997
Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)J Brown, J H Fingert, C M Taylor, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1991
Identification of a germ-line mutation in the p53 gene in a patient with an intracranial ependymomaA K Metzger, V C Sheffield, G Duyk, et al.
American Journal of Human Genetics|March 1, 1992
Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesisP H Cogen, L Daneshvar, A K Metzger, et al.
American Journal of Human Genetics|March 1, 1992
Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, J S Beck, B Nichols, et al.
Nucleic Acids Research|February 25, 1982
Construction and partial characterization of two recombinant cDNA clones for procollagen from chicken cartilageE Vuorio, L Sandell, D Kravis, et al.
Ophthalmology|August 1, 1994
Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosaG A Fishman, E Stone, L D Gilbert, et al.
Pageof 16