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G Brunner

Showing results (421-430 of 727) with videos related to

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European Journal of Human Genetics : EJHG|October 23, 2003
No evidence for involvement of IL-4R and CD11B from the IBD1 region and STAT6 in the IBD2 region in Crohn's diseaseDirk J de Jong, Barbara Franke, Anton H J Naber, et al.
American Journal of Human Genetics|March 31, 2015
Mutations in DVL1 cause an osteosclerotic form of Robinow syndromeKieran J Bunn, Phil Daniel, Heleen S Rösken, et al.
Transplantation|October 3, 2000
Increased glomerular deposits of von Willebrand factor in chronic, but not acute, rejection of primate renal allograftsA S Lagoo, P J Buckley, L J Burchell, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|December 22, 2007
The impact of a false-positive MRI on the choice for mastectomy in BRCA mutation carriers is limitedN Hoogerbrugge, Y J L Kamm, P Bult, et al.
Genomics|September 19, 2003
Cloning, characterization, and mRNA expression analysis of novel human fetal cochlear cDNAsM W J Luijendijk, T J R van de Pol, G van Duijnhoven, et al.
Clinical Genetics|April 11, 2014
De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotypeM Roifman, C L M Marcelis, T Paton, et al.
Journal of Medical Genetics|September 10, 2003
A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated populationS Yzer, L I van den Born, J Schuil, et al.
Neurology|April 26, 2001
Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain diseaseB Cormand, H Pihko, M Bayés, et al.
Canadian Journal of Gastroenterology = Journal Canadien De Gastroenterologie|February 15, 2000
Omeprazole and ranitidine in the prevention of relapse in patients with duodenal ulcer diseaseK Lauritsen, K Rutgersson, E Bolling, et al.
Developmental Medicine and Child Neurology|July 11, 2021
Genetic convergence of developmental and epileptic encephalopathies and intellectual disabilityGemma L Carvill, Sandra Jansen, Amy Lacroix, et al.
Pageof 73

Showing results (421-430 of 727) with videos related to

Sort By:
Pageof 73
European Journal of Human Genetics : EJHG|October 23, 2003
No evidence for involvement of IL-4R and CD11B from the IBD1 region and STAT6 in the IBD2 region in Crohn's diseaseDirk J de Jong, Barbara Franke, Anton H J Naber, et al.
American Journal of Human Genetics|March 31, 2015
Mutations in DVL1 cause an osteosclerotic form of Robinow syndromeKieran J Bunn, Phil Daniel, Heleen S Rösken, et al.
Transplantation|October 3, 2000
Increased glomerular deposits of von Willebrand factor in chronic, but not acute, rejection of primate renal allograftsA S Lagoo, P J Buckley, L J Burchell, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|December 22, 2007
The impact of a false-positive MRI on the choice for mastectomy in BRCA mutation carriers is limitedN Hoogerbrugge, Y J L Kamm, P Bult, et al.
Genomics|September 19, 2003
Cloning, characterization, and mRNA expression analysis of novel human fetal cochlear cDNAsM W J Luijendijk, T J R van de Pol, G van Duijnhoven, et al.
Clinical Genetics|April 11, 2014
De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotypeM Roifman, C L M Marcelis, T Paton, et al.
Journal of Medical Genetics|September 10, 2003
A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated populationS Yzer, L I van den Born, J Schuil, et al.
Neurology|April 26, 2001
Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain diseaseB Cormand, H Pihko, M Bayés, et al.
Canadian Journal of Gastroenterology = Journal Canadien De Gastroenterologie|February 15, 2000
Omeprazole and ranitidine in the prevention of relapse in patients with duodenal ulcer diseaseK Lauritsen, K Rutgersson, E Bolling, et al.
Developmental Medicine and Child Neurology|July 11, 2021
Genetic convergence of developmental and epileptic encephalopathies and intellectual disabilityGemma L Carvill, Sandra Jansen, Amy Lacroix, et al.
Pageof 73