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Han G Brunner

Showing results (81-90 of 318) with videos related to

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American Journal of Human Genetics|April 16, 2002
High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridizationJoris A Veltman, Eric F P M Schoenmakers, Bert H Eussen, et al.
European Journal of Human Genetics : EJHG|January 31, 2008
Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasiaAnnemarie H van der Hout, Grétel G Oudesluijs, Andrea Venema, et al.
Frontiers in Genetics|May 13, 2022
Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect CasesDinu Antony, Elif Gulec Yilmaz, Alper Gezdirici, et al.
Epidemiology (Cambridge, Mass.)|January 8, 2015
Parental subfertility, fertility treatment, and the risk of congenital anorectal malformationsCharlotte H W Wijers, Iris A L M van Rooij, Roxana Rassouli, et al.
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.
Human Mutation|September 10, 2019
Mutations in RPSA and NKX2-3 link development of the spleen and intestinal vasculatureChantal Kerkhofs, Servi J C Stevens, Saul N Faust, 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.
Annals of the Rheumatic Diseases|August 13, 2014
Estimation of heritability of different outcomes for genetic studies of TNFi response in patients with rheumatoid arthritisMaša Umićević Mirkov, Luc Janss, Sita H Vermeulen, et al.
European Journal of Human Genetics : EJHG|March 27, 2021
Correction: Long-read trio sequencing of individuals with unsolved intellectual disabilityMarc Pauper, Erdi Kucuk, Aaron M Wenger, et al.
Pageof 32

Showing results (81-90 of 318) with videos related to

Sort By:
Pageof 32
American Journal of Human Genetics|April 16, 2002
High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridizationJoris A Veltman, Eric F P M Schoenmakers, Bert H Eussen, et al.
European Journal of Human Genetics : EJHG|January 31, 2008
Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasiaAnnemarie H van der Hout, Grétel G Oudesluijs, Andrea Venema, et al.
Frontiers in Genetics|May 13, 2022
Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect CasesDinu Antony, Elif Gulec Yilmaz, Alper Gezdirici, et al.
Epidemiology (Cambridge, Mass.)|January 8, 2015
Parental subfertility, fertility treatment, and the risk of congenital anorectal malformationsCharlotte H W Wijers, Iris A L M van Rooij, Roxana Rassouli, et al.
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.
Human Mutation|September 10, 2019
Mutations in RPSA and NKX2-3 link development of the spleen and intestinal vasculatureChantal Kerkhofs, Servi J C Stevens, Saul N Faust, 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.
Annals of the Rheumatic Diseases|August 13, 2014
Estimation of heritability of different outcomes for genetic studies of TNFi response in patients with rheumatoid arthritisMaša Umićević Mirkov, Luc Janss, Sita H Vermeulen, et al.
European Journal of Human Genetics : EJHG|March 27, 2021
Correction: Long-read trio sequencing of individuals with unsolved intellectual disabilityMarc Pauper, Erdi Kucuk, Aaron M Wenger, et al.
Pageof 32