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K Buiting

Showing results (11-20 of 65) with videos related to

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American Journal of Human Genetics|November 21, 2000
The 28-kb deletion spanning D15S63 is a polymorphic variant in the Ashkenazi Jewish populationS Silverstein, I Lerer, K Buiting, et al.
Human Genetics|November 1, 1994
An insertion/deletion polymorphism at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13B Dittrich, K Buiting, S Gross, et al.
Human Molecular Genetics|September 1, 1993
An NciI RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13B Dittrich, S Gross, K Buiting, et al.
Genomics|April 1, 1993
Characterization of a DNA sequence family in the Prader-Willi/Angelman syndrome chromosome region in 15q11-q13B Dittrich, H Knoblauch, K Buiting, et al.
Genomics|April 28, 2000
Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15C Färber, S Gross, J Neesen, et al.
European Journal of Human Genetics : EJHG|March 1, 1997
A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locusM Zeschnigk, C Lich, K Buiting, et al.
Cytogenetics and Cell Genetics|January 1, 1997
The murine Ext1 gene shows a high level of sequence similarity with its human homologue and is part of a conserved linkage group on chromosome 15D R Lohmann, K Buiting, H J Lüdecke, et al.
Cytogenetics and Cell Genetics|January 21, 2000
The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11-->q13K Buiting, C Körner, B Ulrich, et al.
Human Genetics|January 27, 2000
A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bpK Buiting, C Lich, S Cottrell, et al.
Nature Genetics|August 11, 1998
Methylation analysis of the PWS/AS region does not support an enhancer-competition modelA Schumacher, K Buiting, M Zeschnigk, et al.
Pageof 7

Showing results (11-20 of 65) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|November 21, 2000
The 28-kb deletion spanning D15S63 is a polymorphic variant in the Ashkenazi Jewish populationS Silverstein, I Lerer, K Buiting, et al.
Human Genetics|November 1, 1994
An insertion/deletion polymorphism at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13B Dittrich, K Buiting, S Gross, et al.
Human Molecular Genetics|September 1, 1993
An NciI RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13B Dittrich, S Gross, K Buiting, et al.
Genomics|April 1, 1993
Characterization of a DNA sequence family in the Prader-Willi/Angelman syndrome chromosome region in 15q11-q13B Dittrich, H Knoblauch, K Buiting, et al.
Genomics|April 28, 2000
Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15C Färber, S Gross, J Neesen, et al.
European Journal of Human Genetics : EJHG|March 1, 1997
A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locusM Zeschnigk, C Lich, K Buiting, et al.
Cytogenetics and Cell Genetics|January 1, 1997
The murine Ext1 gene shows a high level of sequence similarity with its human homologue and is part of a conserved linkage group on chromosome 15D R Lohmann, K Buiting, H J Lüdecke, et al.
Cytogenetics and Cell Genetics|January 21, 2000
The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11-->q13K Buiting, C Körner, B Ulrich, et al.
Human Genetics|January 27, 2000
A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bpK Buiting, C Lich, S Cottrell, et al.
Nature Genetics|August 11, 1998
Methylation analysis of the PWS/AS region does not support an enhancer-competition modelA Schumacher, K Buiting, M Zeschnigk, et al.
Pageof 7