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Human Molecular Genetics
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October 1, 1994
Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
R Wevrick, J A Kerns, U Francke
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale
|
July 27, 2000
Deconstructing Mendel: new paradigms in genetic mechanisms
D 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 syndrome
R Wevrick, J A Kerns, U Francke
Human Molecular Genetics
|
June 1, 1993
Cloning and analysis of the murine Fanconi anemia group C cDNA
R 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 clusters
M 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 orthologues
T 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 7
R 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 DNA
H F Willard, R Wevrick, P E Warburton
Nature Genetics
|
October 3, 1999
Disruption of the mouse necdin gene results in early post-natal lethality
M 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 satellite
P E Warburton, R Wevrick, M M Mahtani, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
Human Molecular Genetics
|
October 1, 1994
Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
R Wevrick, J A Kerns, U Francke
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale
|
July 27, 2000
Deconstructing Mendel: new paradigms in genetic mechanisms
D 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 syndrome
R Wevrick, J A Kerns, U Francke
Human Molecular Genetics
|
June 1, 1993
Cloning and analysis of the murine Fanconi anemia group C cDNA
R 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 clusters
M 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 orthologues
T 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 7
R 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 DNA
H F Willard, R Wevrick, P E Warburton
Nature Genetics
|
October 3, 1999
Disruption of the mouse necdin gene results in early post-natal lethality
M 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 satellite
P E Warburton, R Wevrick, M M Mahtani, et al.
Page
of 3