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Human Molecular Genetics|September 25, 1997
The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouseH R MacDonald, R WevrickClinical Genetics|March 22, 2001
The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndromeM L Hanel, R WevrickProceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stabilityR Wevrick, H F WillardHuman Molecular Genetics|October 1, 1994
Identification of a novel paternally expressed gene in the Prader-Willi syndrome regionR Wevrick, J A Kerns, U FranckeClinical and Investigative Medicine. Medecine Clinique Et Experimentale|July 27, 2000
Deconstructing Mendel: new paradigms in genetic mechanismsD Gilchrist, D M Glerum, R WevrickCytogenetics 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 WevrickBMC 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 WevrickGenomics|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 WillardNature Genetics|October 3, 1999
Disruption of the mouse necdin gene results in early post-natal lethalityM Gérard, L Hernandez, R Wevrick, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1976
Abnormal levels of 3':5'-cyclic AMP in isoproterenol-stimulated fibroblasts from patients with cystic fibrosisM BuchwaldPageof 15