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R Wevrick

Showing results (1-10 of 27) with videos related to

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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 Wevrick
Human Molecular Genetics|February 1, 1997
An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) geneR Wevrick, U Francke
Current Opinion in Genetics & Development|June 1, 1993
Mammalian DNA-repair genesR Wevrick, M Buchwald
Lancet (London, England)|October 19, 1996
Diagnostic test for the Prader-Willi syndrome by SNRPN expression in bloodR Wevrick, U Francke
Molecular 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 Wevrick
Clinical 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 Wevrick
Nucleic 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 Willard
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 Wevrick
Clinical Genetics|March 22, 2001
The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndromeM L Hanel, R Wevrick
Proceedings 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 Willard
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
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 Wevrick
Human Molecular Genetics|February 1, 1997
An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) geneR Wevrick, U Francke
Current Opinion in Genetics & Development|June 1, 1993
Mammalian DNA-repair genesR Wevrick, M Buchwald
Lancet (London, England)|October 19, 1996
Diagnostic test for the Prader-Willi syndrome by SNRPN expression in bloodR Wevrick, U Francke
Molecular 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 Wevrick
Clinical 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 Wevrick
Nucleic 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 Willard
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 Wevrick
Clinical Genetics|March 22, 2001
The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndromeM L Hanel, R Wevrick
Proceedings 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 Willard
Pageof 3