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Showing results (191-200 of 305) with videos related to

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European Journal of Human Genetics : EJHG|February 4, 2016
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndromeJasmin Beygo, Ivana Joksic, Tim M Strom, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2000
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organizationJ Cavaillé, K Buiting, M Kiefmann, et al.
BMJ Open|November 27, 2015
Bereaved relatives' experiences during the incurable phase of cancer: a qualitative interview studyMarleen N Wijnhoven, Wim E Terpstra, Ronald van Rossem, et al.
American Journal of Medical Genetics. Part A|May 15, 2007
Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup-shaped ears, congenital heart defect, and mental retardation--new MCA/MR syndrome in two affected sibs and a mildly affected mother?Dagmar Wieczorek, Charles Shaw-Smith, Jürgen Kohlhase, et al.
The Netherlands Journal of Medicine|February 13, 2001
BCG immunotherapy: be cautious of granulomas. Disseminated BCG infection and mycotic aneurysm as late complications of intravesical BCG instillationsJ T Kamphuis, A G Buiting, J F Miseré, et al.
Human Molecular Genetics|August 29, 2003
Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genesBernhard Horsthemke, Hülya Nazlican, Johannes Hüsing, et al.
Molecular Syndromology|June 20, 2012
First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins SyndromeJ Beygo, K Buiting, S Seland, et al.
Critical Care Medicine|December 11, 2014
The role of systemic antibiotics in acquiring respiratory tract colonization with gram-negative bacteria in intensive care patients: a nested cohort studyIrene P Jongerden, Ben Speelberg, Claudia L Satizábal, et al.
Critical Care Medicine|March 2, 2011
Effect of open and closed endotracheal suctioning on cross-transmission with Gram-negative bacteria: a prospective crossover studyIrene P Jongerden, Anton G Buiting, Maurine A Leverstein-van Hall, et al.
Journal of Clinical Microbiology|January 16, 1999
Molecular genotyping of Staphylococcus aureus strains: comparison of repetitive element sequence-based PCR with various typing methods and isolation of a novel epidemicity markerA van der Zee, H Verbakel, J C van Zon, et al.
Pageof 31

Showing results (191-200 of 305) with videos related to

Sort By:
Pageof 31
European Journal of Human Genetics : EJHG|February 4, 2016
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndromeJasmin Beygo, Ivana Joksic, Tim M Strom, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2000
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organizationJ Cavaillé, K Buiting, M Kiefmann, et al.
BMJ Open|November 27, 2015
Bereaved relatives' experiences during the incurable phase of cancer: a qualitative interview studyMarleen N Wijnhoven, Wim E Terpstra, Ronald van Rossem, et al.
American Journal of Medical Genetics. Part A|May 15, 2007
Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup-shaped ears, congenital heart defect, and mental retardation--new MCA/MR syndrome in two affected sibs and a mildly affected mother?Dagmar Wieczorek, Charles Shaw-Smith, Jürgen Kohlhase, et al.
The Netherlands Journal of Medicine|February 13, 2001
BCG immunotherapy: be cautious of granulomas. Disseminated BCG infection and mycotic aneurysm as late complications of intravesical BCG instillationsJ T Kamphuis, A G Buiting, J F Miseré, et al.
Human Molecular Genetics|August 29, 2003
Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genesBernhard Horsthemke, Hülya Nazlican, Johannes Hüsing, et al.
Molecular Syndromology|June 20, 2012
First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins SyndromeJ Beygo, K Buiting, S Seland, et al.
Critical Care Medicine|December 11, 2014
The role of systemic antibiotics in acquiring respiratory tract colonization with gram-negative bacteria in intensive care patients: a nested cohort studyIrene P Jongerden, Ben Speelberg, Claudia L Satizábal, et al.
Critical Care Medicine|March 2, 2011
Effect of open and closed endotracheal suctioning on cross-transmission with Gram-negative bacteria: a prospective crossover studyIrene P Jongerden, Anton G Buiting, Maurine A Leverstein-van Hall, et al.
Journal of Clinical Microbiology|January 16, 1999
Molecular genotyping of Staphylococcus aureus strains: comparison of repetitive element sequence-based PCR with various typing methods and isolation of a novel epidemicity markerA van der Zee, H Verbakel, J C van Zon, et al.
Pageof 31