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Showing results (61-70 of 153) with videos related to

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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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1994
Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6qE M Stone, B E Nichols, A E Kimura, et al.
Gene|November 24, 1999
Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1)N B Haider, C Searby, E Galperin, et al.
Human Genetics|March 1, 1993
A denaturing gradient gel electrophoresis assay for sensitive detection of p53 mutationsJ S Beck, A E Kwitek, P H Cogen, 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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1992
Procollagen II gene mutation in Stickler syndromeD M Brown, B E Nichols, T A Weingeist, et al.
JAMA|June 22, 1999
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafnessG E Green, D A Scott, J M McDonald, et al.
The American Journal of Pathology|September 1, 1995
Microsatellite instability in adenocarcinoma of the prostateR B Terrell, A H Wille, J C Cheville, et al.
Pageof 16

Showing results (61-70 of 153) with videos related to

Sort By:
Pageof 16
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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1994
Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6qE M Stone, B E Nichols, A E Kimura, et al.
Gene|November 24, 1999
Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1)N B Haider, C Searby, E Galperin, et al.
Human Genetics|March 1, 1993
A denaturing gradient gel electrophoresis assay for sensitive detection of p53 mutationsJ S Beck, A E Kwitek, P H Cogen, 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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1992
Procollagen II gene mutation in Stickler syndromeD M Brown, B E Nichols, T A Weingeist, et al.
JAMA|June 22, 1999
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafnessG E Green, D A Scott, J M McDonald, et al.
The American Journal of Pathology|September 1, 1995
Microsatellite instability in adenocarcinoma of the prostateR B Terrell, A H Wille, J C Cheville, et al.
Pageof 16