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Showing results (201-210 of 305) with videos related to

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Molecular Genetics & Genomic Medicine|November 28, 2017
The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?Thomas Eggermann, Barbara Oehl-Jaschkowitz, Severin Dicks, et al.
Human Genetics|March 12, 2004
SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndromeMaren Runte, Peter M Kroisel, Gabriele Gillessen-Kaesbach, et al.
European Journal of Human Genetics : EJHG|December 27, 2007
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasiaMichael Zeschnigk, Beate Albrecht, Karin Buiting, et al.
Plos One|May 19, 2020
Within-patient plasmid dynamics in Klebsiella pneumoniae during an outbreak of a carbapenemase-producing Klebsiella pneumoniaeJoep J J M Stohr, Jaco J Verweij, Anton G M Buiting, et al.
Epigenetics|December 3, 2016
Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domainsDavid Monk, Joannella Morales, Johan T den Dunnen, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 26, 2003
[Optimalization of antibiotic policy in the Netherlands. VII. SWAB-guidelines for antimicrobial therapy in adults patients with infectious endocarditis]D W Verhagen, M van der Feltz, H W Plokker, et al.
Journal of Clinical Microbiology|October 7, 2005
Outbreak of infection with a multiresistant Klebsiella pneumoniae strain associated with contaminated roll boards in operating roomsAnnemarie van 't Veen, Anneke van der Zee, Jolande Nelson, et al.
Human Molecular Genetics|February 19, 2009
Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incompleteMichael Zeschnigk, Marcel Martin, Gisela Betzl, et al.
Journal of the Endocrine Society|July 10, 2019
Resistance to GHRH but Not to PTH in a 15-Year-Old Boy With Pseudohypoparathyroidism 1AMartin Munteanu, Cordula Kiewert, Nora Matar, 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.
Pageof 31

Showing results (201-210 of 305) with videos related to

Sort By:
Pageof 31
Molecular Genetics & Genomic Medicine|November 28, 2017
The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?Thomas Eggermann, Barbara Oehl-Jaschkowitz, Severin Dicks, et al.
Human Genetics|March 12, 2004
SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndromeMaren Runte, Peter M Kroisel, Gabriele Gillessen-Kaesbach, et al.
European Journal of Human Genetics : EJHG|December 27, 2007
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasiaMichael Zeschnigk, Beate Albrecht, Karin Buiting, et al.
Plos One|May 19, 2020
Within-patient plasmid dynamics in Klebsiella pneumoniae during an outbreak of a carbapenemase-producing Klebsiella pneumoniaeJoep J J M Stohr, Jaco J Verweij, Anton G M Buiting, et al.
Epigenetics|December 3, 2016
Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domainsDavid Monk, Joannella Morales, Johan T den Dunnen, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 26, 2003
[Optimalization of antibiotic policy in the Netherlands. VII. SWAB-guidelines for antimicrobial therapy in adults patients with infectious endocarditis]D W Verhagen, M van der Feltz, H W Plokker, et al.
Journal of Clinical Microbiology|October 7, 2005
Outbreak of infection with a multiresistant Klebsiella pneumoniae strain associated with contaminated roll boards in operating roomsAnnemarie van 't Veen, Anneke van der Zee, Jolande Nelson, et al.
Human Molecular Genetics|February 19, 2009
Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incompleteMichael Zeschnigk, Marcel Martin, Gisela Betzl, et al.
Journal of the Endocrine Society|July 10, 2019
Resistance to GHRH but Not to PTH in a 15-Year-Old Boy With Pseudohypoparathyroidism 1AMartin Munteanu, Cordula Kiewert, Nora Matar, 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.
Pageof 31