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K Buiting

Showing results (41-50 of 65) with videos related to

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Human Molecular Genetics|December 1, 1993
Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN geneK Buiting, B Dittrich, S Gross, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 15, 1992
A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromesK Buiting, V Greger, B H Brownstein, et al.
Klinische Padiatrie|November 9, 2010
Malignant melanoma and Wiedemann-Beckwith syndrome in childhoodE Livingstone, A Caliebe, F Egberts, et al.
American Journal of Human Genetics|January 29, 2003
Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injectionK H Ørstavik, K Eiklid, C B van der Hagen, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2000
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organizationJ Cavaillé, K Buiting, M Kiefmann, et al.
Molecular Syndromology|June 20, 2012
First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins SyndromeJ Beygo, K Buiting, S Seland, et al.
Human Molecular Genetics|September 1, 1992
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysisA Kuwano, A Mutirangura, B Dittrich, et al.
American Journal of Human Genetics|August 1, 1997
Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndromeJ M Conroy, T A Grebe, L A Becker, et al.
Nature Genetics|October 1, 1996
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneB Dittrich, K Buiting, B Korn, et al.
American Journal of Human Genetics|February 11, 1999
Molecular mechanism of angelman syndrome in two large families involves an imprinting mutationT Ohta, K Buiting, H Kokkonen, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|December 1, 1993
Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN geneK Buiting, B Dittrich, S Gross, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 15, 1992
A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromesK Buiting, V Greger, B H Brownstein, et al.
Klinische Padiatrie|November 9, 2010
Malignant melanoma and Wiedemann-Beckwith syndrome in childhoodE Livingstone, A Caliebe, F Egberts, et al.
American Journal of Human Genetics|January 29, 2003
Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injectionK H Ørstavik, K Eiklid, C B van der Hagen, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2000
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organizationJ Cavaillé, K Buiting, M Kiefmann, et al.
Molecular Syndromology|June 20, 2012
First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins SyndromeJ Beygo, K Buiting, S Seland, et al.
Human Molecular Genetics|September 1, 1992
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysisA Kuwano, A Mutirangura, B Dittrich, et al.
American Journal of Human Genetics|August 1, 1997
Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndromeJ M Conroy, T A Grebe, L A Becker, et al.
Nature Genetics|October 1, 1996
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneB Dittrich, K Buiting, B Korn, et al.
American Journal of Human Genetics|February 11, 1999
Molecular mechanism of angelman syndrome in two large families involves an imprinting mutationT Ohta, K Buiting, H Kokkonen, et al.
Pageof 7