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G Brunner

Showing results (371-380 of 727) with videos related to

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Human Mutation|November 16, 2005
Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing lossE Kalay, A Karaguzel, R Caylan, et al.
American Journal of Human Genetics|October 23, 2008
Recurrent CNVs disrupt three candidate genes in schizophrenia patientsTerry Vrijenhoek, Jacobine E Buizer-Voskamp, Inge van der Stelt, et al.
Clinical Genetics|January 26, 2010
Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndromeJ F Mazzeu, A M Vianna-Morgante, A C V Krepischi, et al.
European Journal of Human Genetics : EJHG|October 7, 2018
1 in 38 individuals at risk of a dominant medically actionable diseaseLonneke Haer-Wigman, Vyne van der Schoot, Ilse Feenstra, et al.
Human Genetics|February 1, 1991
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosisB A van Oost, P M van Zandvoort, W Tünte, et al.
Orphanet Journal of Rare Diseases|September 19, 2015
Meier-Gorlin syndromeSonja A de Munnik, Elisabeth H Hoefsloot, Jolt Roukema, et al.
The EMBO Journal|April 1, 1994
Release of GPI-anchored membrane proteins by a cell-associated GPI-specific phospholipase DC N Metz, G Brunner, N H Choi-Muira, et al.
European Journal of Human Genetics : EJHG|August 17, 2006
Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genesCaroline B Michielse, Meena Bhat, Angela Brady, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|November 2, 2002
PLEXIN-D1, a novel plexin family member, is expressed in vascular endothelium and the central nervous system during mouse embryogenesisBert van der Zwaag, Anita J C G M Hellemons, William P J Leenders, et al.
Antimicrobial Agents and Chemotherapy|October 8, 2008
Glycerol monolaurate does not alter rhesus macaque (Macaca mulatta) vaginal lactobacilli and is safe for chronic usePatrick M Schlievert, Kristi L Strandberg, Amanda J Brosnahan, et al.
Pageof 73

Showing results (371-380 of 727) with videos related to

Sort By:
Pageof 73
Human Mutation|November 16, 2005
Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing lossE Kalay, A Karaguzel, R Caylan, et al.
American Journal of Human Genetics|October 23, 2008
Recurrent CNVs disrupt three candidate genes in schizophrenia patientsTerry Vrijenhoek, Jacobine E Buizer-Voskamp, Inge van der Stelt, et al.
Clinical Genetics|January 26, 2010
Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndromeJ F Mazzeu, A M Vianna-Morgante, A C V Krepischi, et al.
European Journal of Human Genetics : EJHG|October 7, 2018
1 in 38 individuals at risk of a dominant medically actionable diseaseLonneke Haer-Wigman, Vyne van der Schoot, Ilse Feenstra, et al.
Human Genetics|February 1, 1991
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosisB A van Oost, P M van Zandvoort, W Tünte, et al.
Orphanet Journal of Rare Diseases|September 19, 2015
Meier-Gorlin syndromeSonja A de Munnik, Elisabeth H Hoefsloot, Jolt Roukema, et al.
The EMBO Journal|April 1, 1994
Release of GPI-anchored membrane proteins by a cell-associated GPI-specific phospholipase DC N Metz, G Brunner, N H Choi-Muira, et al.
European Journal of Human Genetics : EJHG|August 17, 2006
Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genesCaroline B Michielse, Meena Bhat, Angela Brady, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|November 2, 2002
PLEXIN-D1, a novel plexin family member, is expressed in vascular endothelium and the central nervous system during mouse embryogenesisBert van der Zwaag, Anita J C G M Hellemons, William P J Leenders, et al.
Antimicrobial Agents and Chemotherapy|October 8, 2008
Glycerol monolaurate does not alter rhesus macaque (Macaca mulatta) vaginal lactobacilli and is safe for chronic usePatrick M Schlievert, Kristi L Strandberg, Amanda J Brosnahan, et al.
Pageof 73