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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 syndrome
Jasmin 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 organization
J Cavaillé, K Buiting, M Kiefmann, et al.
BMJ Open
|
November 27, 2015
Bereaved relatives' experiences during the incurable phase of cancer: a qualitative interview study
Marleen 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 instillations
J 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 genes
Bernhard Horsthemke, Hülya Nazlican, Johannes Hüsing, et al.
Molecular Syndromology
|
June 20, 2012
First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome
J 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 study
Irene 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 study
Irene 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 marker
A van der Zee, H Verbakel, J C van Zon, et al.
Page
of 31
Search research articles
Search
Showing results (191-200 of 305) with videos related to
Sort By:
Page
of 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 syndrome
Jasmin 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 organization
J Cavaillé, K Buiting, M Kiefmann, et al.
BMJ Open
|
November 27, 2015
Bereaved relatives' experiences during the incurable phase of cancer: a qualitative interview study
Marleen 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 instillations
J 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 genes
Bernhard Horsthemke, Hülya Nazlican, Johannes Hüsing, et al.
Molecular Syndromology
|
June 20, 2012
First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome
J 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 study
Irene 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 study
Irene 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 marker
A van der Zee, H Verbakel, J C van Zon, et al.
Page
of 31