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Showing results (171-180 of 305) with videos related to

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Human Molecular Genetics|October 23, 2014
Epigenetic germline mosaicism in infertile menSandra Laurentino, Jasmin Beygo, Verena Nordhoff, et al.
Klinische Padiatrie|November 9, 2010
Malignant melanoma and Wiedemann-Beckwith syndrome in childhoodE Livingstone, A Caliebe, F Egberts, et al.
Plos Genetics|December 31, 2009
The human retinoblastoma gene is imprintedDeniz Kanber, Tea Berulava, Ole Ammerpohl, 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.
BMJ (Clinical Research Ed.)|March 18, 2008
Continuous deep sedation for patients nearing death in the Netherlands: descriptive studyJudith Rietjens, Johannes van Delden, Bregje Onwuteaka-Philipsen, et al.
Journal of Animal Science|August 1, 1995
Genetics of the interval from weaning to estrus in first-litter sows: distribution of data, direct response of selection, and heritabilityJ ten Napel, A G de Vries, G A Buiting, et al.
European Journal of Human Genetics : EJHG|April 11, 2013
Evidence for anticipation in Beckwith-Wiedemann syndromeSiren Berland, Mia Appelbäck, Ove Bruland, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
Atypical Angelman syndrome due to a mosaic imprinting defect: Case reports and review of the literatureAnna Le Fevre, Jasmin Beygo, Cheryl Silveira, et al.
BMJ Open|May 20, 2015
Analytical performance, agreement and user-friendliness of six point-of-care testing urine analysers for urinary tract infection in general practiceMarjolein J C Schot, Sanne van Delft, Antoinette M J Kooijman-Buiting, et al.
American Journal of Medical Genetics. Part A|July 6, 2010
Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14Melita D Irving, Karin Buiting, Deniz Kanber, et al.
Pageof 31

Showing results (171-180 of 305) with videos related to

Sort By:
Pageof 31
Human Molecular Genetics|October 23, 2014
Epigenetic germline mosaicism in infertile menSandra Laurentino, Jasmin Beygo, Verena Nordhoff, et al.
Klinische Padiatrie|November 9, 2010
Malignant melanoma and Wiedemann-Beckwith syndrome in childhoodE Livingstone, A Caliebe, F Egberts, et al.
Plos Genetics|December 31, 2009
The human retinoblastoma gene is imprintedDeniz Kanber, Tea Berulava, Ole Ammerpohl, 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.
BMJ (Clinical Research Ed.)|March 18, 2008
Continuous deep sedation for patients nearing death in the Netherlands: descriptive studyJudith Rietjens, Johannes van Delden, Bregje Onwuteaka-Philipsen, et al.
Journal of Animal Science|August 1, 1995
Genetics of the interval from weaning to estrus in first-litter sows: distribution of data, direct response of selection, and heritabilityJ ten Napel, A G de Vries, G A Buiting, et al.
European Journal of Human Genetics : EJHG|April 11, 2013
Evidence for anticipation in Beckwith-Wiedemann syndromeSiren Berland, Mia Appelbäck, Ove Bruland, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
Atypical Angelman syndrome due to a mosaic imprinting defect: Case reports and review of the literatureAnna Le Fevre, Jasmin Beygo, Cheryl Silveira, et al.
BMJ Open|May 20, 2015
Analytical performance, agreement and user-friendliness of six point-of-care testing urine analysers for urinary tract infection in general practiceMarjolein J C Schot, Sanne van Delft, Antoinette M J Kooijman-Buiting, et al.
American Journal of Medical Genetics. Part A|July 6, 2010
Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14Melita D Irving, Karin Buiting, Deniz Kanber, et al.
Pageof 31