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Current Opinion in Genetics & Development|June 1, 1993
Mammalian DNA-repair genesR Wevrick, M BuchwaldHuman Molecular Genetics|June 1, 1993
Cloning and analysis of the murine Fanconi anemia group C cDNAR Wevrick, C A Clarke, M BuchwaldMammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Mapping of the murine and rat Facc genes and assessment of flexed-tail as a candidate mouse homolog of Fanconi anemia group CR Wevrick, J E Barker, J H Nadeau, et al.Blood Cells, Molecules & Diseases|January 1, 1995
Expression of the Fanconi anemia gene FAC in human cell lines: lack of effect of oxygen tensionH Joenje, H Youssoufian, F A Kruyt, et al.American Journal of Human Genetics|March 11, 2000
Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting controlS Lee, R WevrickHuman Molecular Genetics|February 1, 1997
An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) geneR Wevrick, U FranckeLancet (London, England)|October 19, 1996
Diagnostic test for the Prader-Willi syndrome by SNRPN expression in bloodR Wevrick, U FranckeMolecular and Cellular Biology|March 22, 2001
Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting centerM L Hanel, R WevrickClinical Genetics|April 27, 2012
Co-morbidity of complex genetic disorders and hypersomnias of central origin: lessons from the underlying neurobiology of wake and sleepS V Weselake, R WevrickNucleic Acids Research|May 11, 1991
Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arraysR Wevrick, H F WillardPageof 15