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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 syndrome
Maren 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 hemihypoplasia
Michael 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 pneumoniae
Joep 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 domains
David 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 rooms
Annemarie 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 incomplete
Michael 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 1A
Martin 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 syndrome
J M Conroy, T A Grebe, L A Becker, et al.
Page
of 31
Search research articles
Search
Showing results (201-210 of 305) with videos related to
Sort By:
Page
of 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 syndrome
Maren 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 hemihypoplasia
Michael 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 pneumoniae
Joep 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 domains
David 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 rooms
Annemarie 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 incomplete
Michael 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 1A
Martin 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 syndrome
J M Conroy, T A Grebe, L A Becker, et al.
Page
of 31