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K Buiting

Showing results (1-10 of 65) with videos related to

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Cytogenetic and Genome Research|April 1, 2006
Imprinting defects on human chromosome 15B Horsthemke, K Buiting
American Journal of Medical Genetics|January 11, 1996
PW71 methylation test for Prader-Willi and Angelman syndromesB Dittrich, K Buiting, B Horsthemke
Human Mutation|January 1, 1997
Imprinting mutations on human chromosome 15B Horsthemke, B Dittrich, K Buiting
Genomics|August 1, 1988
Construction of a chromosome 15-specific linking library and identification of potential gene sequencesK Buiting, E Passarge, B Horsthemke
Cytogenetics and Cell Genetics|January 1, 1996
A pseudogene for the human ribosomal protein L5 (RPL5P1) maps within an intron of the SNRPN transcription unit on human chromosome 15K Buiting, S Kaya-Westerloh, B Horsthemke
Molecular Syndromology|June 7, 2012
Molecular and Clinical Aspects of Angelman SyndromeA Dagli, K Buiting, C A Williams
Proceedings of the National Academy of Sciences of the United States of America|March 21, 1998
Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic DrosophilaF Lyko, K Buiting, B Horsthemke, et al.
Human Molecular Genetics|February 5, 1999
The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletionC Färber, B Dittrich, K Buiting, et al.
Genomics|February 15, 1997
Identification of novel exons 3' to the human SNRPN geneK Buiting, B Dittrich, S Endele, et al.
Human Molecular Genetics|December 1, 1993
Characterization of a methylation imprint in the Prader-Willi syndrome chromosome regionB Dittrich, K Buiting, S Gross, et al.
Pageof 7

Showing results (1-10 of 65) with videos related to

Sort By:
Pageof 7
Cytogenetic and Genome Research|April 1, 2006
Imprinting defects on human chromosome 15B Horsthemke, K Buiting
American Journal of Medical Genetics|January 11, 1996
PW71 methylation test for Prader-Willi and Angelman syndromesB Dittrich, K Buiting, B Horsthemke
Human Mutation|January 1, 1997
Imprinting mutations on human chromosome 15B Horsthemke, B Dittrich, K Buiting
Genomics|August 1, 1988
Construction of a chromosome 15-specific linking library and identification of potential gene sequencesK Buiting, E Passarge, B Horsthemke
Cytogenetics and Cell Genetics|January 1, 1996
A pseudogene for the human ribosomal protein L5 (RPL5P1) maps within an intron of the SNRPN transcription unit on human chromosome 15K Buiting, S Kaya-Westerloh, B Horsthemke
Molecular Syndromology|June 7, 2012
Molecular and Clinical Aspects of Angelman SyndromeA Dagli, K Buiting, C A Williams
Proceedings of the National Academy of Sciences of the United States of America|March 21, 1998
Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic DrosophilaF Lyko, K Buiting, B Horsthemke, et al.
Human Molecular Genetics|February 5, 1999
The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletionC Färber, B Dittrich, K Buiting, et al.
Genomics|February 15, 1997
Identification of novel exons 3' to the human SNRPN geneK Buiting, B Dittrich, S Endele, et al.
Human Molecular Genetics|December 1, 1993
Characterization of a methylation imprint in the Prader-Willi syndrome chromosome regionB Dittrich, K Buiting, S Gross, et al.
Pageof 7