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R Wevrick

Showing results (11-20 of 27) with videos related to

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Human Molecular Genetics|October 1, 1994
Identification of a novel paternally expressed gene in the Prader-Willi syndrome regionR Wevrick, J A Kerns, U Francke
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|July 27, 2000
Deconstructing Mendel: new paradigms in genetic mechanismsD Gilchrist, D M Glerum, R Wevrick
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
The IPW gene is imprinted and is not expressed in the Prader-Willi syndromeR Wevrick, J A Kerns, U Francke
Human Molecular Genetics|June 1, 1993
Cloning and analysis of the murine Fanconi anemia group C cDNAR Wevrick, C A Clarke, M Buchwald
Cytogenetics and Cell Genetics|April 18, 2001
Analysis of DEXI/Dexi refines the organization of the mouse 7C and human 15q11-->q13 imprinting clustersM Kelly, A J Edgar, R Wevrick
BMC Genetics|January 10, 2002
A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologuesT K Chibuk, J M Bischof, R Wevrick
Genomics|December 1, 1992
Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7R Wevrick, V P Willard, H F Willard
Progress in Clinical and Biological Research|January 1, 1989
Human centromere structure: organization and potential role of alpha satellite DNAH F Willard, R Wevrick, P E Warburton
Nature Genetics|October 3, 1999
Disruption of the mouse necdin gene results in early post-natal lethalityM Gérard, L Hernandez, R Wevrick, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 17, 2011
Pulsed-field and two-dimensional gel electrophoresis of long arrays of tandemly repeated DNA : analysis of human centromeric alpha satelliteP E Warburton, R Wevrick, M M Mahtani, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|October 1, 1994
Identification of a novel paternally expressed gene in the Prader-Willi syndrome regionR Wevrick, J A Kerns, U Francke
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|July 27, 2000
Deconstructing Mendel: new paradigms in genetic mechanismsD Gilchrist, D M Glerum, R Wevrick
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
The IPW gene is imprinted and is not expressed in the Prader-Willi syndromeR Wevrick, J A Kerns, U Francke
Human Molecular Genetics|June 1, 1993
Cloning and analysis of the murine Fanconi anemia group C cDNAR Wevrick, C A Clarke, M Buchwald
Cytogenetics and Cell Genetics|April 18, 2001
Analysis of DEXI/Dexi refines the organization of the mouse 7C and human 15q11-->q13 imprinting clustersM Kelly, A J Edgar, R Wevrick
BMC Genetics|January 10, 2002
A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologuesT K Chibuk, J M Bischof, R Wevrick
Genomics|December 1, 1992
Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7R Wevrick, V P Willard, H F Willard
Progress in Clinical and Biological Research|January 1, 1989
Human centromere structure: organization and potential role of alpha satellite DNAH F Willard, R Wevrick, P E Warburton
Nature Genetics|October 3, 1999
Disruption of the mouse necdin gene results in early post-natal lethalityM Gérard, L Hernandez, R Wevrick, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 17, 2011
Pulsed-field and two-dimensional gel electrophoresis of long arrays of tandemly repeated DNA : analysis of human centromeric alpha satelliteP E Warburton, R Wevrick, M M Mahtani, et al.
Pageof 3