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R Wevrick

Showing results (21-30 of 27) with videos related to

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Molecular and Cellular Biology|December 1, 1990
Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangementR Wevrick, W C Earnshaw, P N Howard-Peebles, et al.
Mammalian 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.
Human Genetics|September 1, 1997
Human centromeric DNAsC Lee, R Wevrick, R B Fisher, 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.
Human Molecular Genetics|August 1, 2000
Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotypeS Lee, S Kozlov, L Hernandez, et al.
Nature Genetics|May 20, 1998
A mouse model for Prader-Willi syndrome imprinting-centre mutationsT Yang, T E Adamson, J L Resnick, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., CanadaW P Robinson, B Horsthemke, S Leonard, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Molecular and Cellular Biology|December 1, 1990
Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangementR Wevrick, W C Earnshaw, P N Howard-Peebles, et al.
Mammalian 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.
Human Genetics|September 1, 1997
Human centromeric DNAsC Lee, R Wevrick, R B Fisher, 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.
Human Molecular Genetics|August 1, 2000
Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotypeS Lee, S Kozlov, L Hernandez, et al.
Nature Genetics|May 20, 1998
A mouse model for Prader-Willi syndrome imprinting-centre mutationsT Yang, T E Adamson, J L Resnick, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., CanadaW P Robinson, B Horsthemke, S Leonard, et al.
Pageof 3