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K Buiting

Showing results (31-40 of 65) with videos related to

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Human Molecular Genetics|June 1, 1994
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implicationsK Buiting, B Dittrich, W P Robinson, et al.
Nature Genetics|April 1, 1995
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15K Buiting, S Saitoh, S Gross, et al.
Human Genetics|November 1, 1992
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13B Dittrich, W P Robinson, H Knoblauch, et al.
Clinical Genetics|December 12, 2007
Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndromeT Eggermann, N Schönherr, K Eggermann, et al.
American Journal of Human Genetics|July 1, 1997
Different mechanisms and recurrence risks of imprinting defects in Angelman syndromeJ Bürger, K Buiting, B Dittrich, et al.
Genomics|March 1, 1990
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequencesK Buiting, M Neumann, H J Lüdecke, et al.
Clinical Genetics|November 15, 2000
Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselingK Buiting, C Färber, P Kroisel, et al.
American Journal of Human Genetics|May 1, 1994
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromesA Reis, B Dittrich, V Greger, et al.
Nature Genetics|May 10, 2000
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switchB Bielinska, S M Blaydes, K Buiting, et al.
Nature Genetics|December 2, 2000
The imprinting box of the Prader-Willi/Angelman syndrome domainR Shemer, A Y Hershko, J Perk, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|June 1, 1994
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implicationsK Buiting, B Dittrich, W P Robinson, et al.
Nature Genetics|April 1, 1995
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15K Buiting, S Saitoh, S Gross, et al.
Human Genetics|November 1, 1992
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13B Dittrich, W P Robinson, H Knoblauch, et al.
Clinical Genetics|December 12, 2007
Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndromeT Eggermann, N Schönherr, K Eggermann, et al.
American Journal of Human Genetics|July 1, 1997
Different mechanisms and recurrence risks of imprinting defects in Angelman syndromeJ Bürger, K Buiting, B Dittrich, et al.
Genomics|March 1, 1990
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequencesK Buiting, M Neumann, H J Lüdecke, et al.
Clinical Genetics|November 15, 2000
Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselingK Buiting, C Färber, P Kroisel, et al.
American Journal of Human Genetics|May 1, 1994
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromesA Reis, B Dittrich, V Greger, et al.
Nature Genetics|May 10, 2000
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switchB Bielinska, S M Blaydes, K Buiting, et al.
Nature Genetics|December 2, 2000
The imprinting box of the Prader-Willi/Angelman syndrome domainR Shemer, A Y Hershko, J Perk, et al.
Pageof 7