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Han G Brunner

Showing results (131-140 of 318) with videos related to

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Human Genetics|April 17, 2007
Intragenic deletion in the LARGE gene causes Walker-Warburg syndromeJeroen van Reeuwijk, Prabhjit K Grewal, Mustafa A M Salih, et al.
Plos Genetics|November 9, 2013
Human intellectual disability genes form conserved functional modules in DrosophilaMerel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, et al.
European Journal of Pediatrics|October 17, 2014
Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadiasRomy van de Putte, Charlotte H W Wijers, Ivo de Blaauw, et al.
Nature Genetics|November 16, 2010
A de novo paradigm for mental retardationLisenka E L M Vissers, Joep de Ligt, Christian Gilissen, et al.
American Journal of Human Genetics|March 24, 2015
Absence of heterozygosity due to template switching during replicative rearrangementsClaudia M B Carvalho, Rolph Pfundt, Daniel A King, et al.
JACC. Heart Failure|August 28, 2023
Clonal Hematopoiesis Has Prognostic Value in Dilated Cardiomyopathy Independent of Age and Clone SizeMaurits A Sikking, Sophie L V M Stroeks, Michiel T H M Henkens, et al.
Journal of Medical Genetics|February 28, 2012
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defectsMarjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, et al.
Journal of Cardiac Failure|September 22, 2019
Metabolic Profiling Associates with Disease Severity in Nonischemic Dilated CardiomyopathyJob A J Verdonschot, Ping Wang, Marc Van Bilsen, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndromeNeil V Morgan, Louise A Brueton, Phillip Cox, et al.
Circulation. Heart Failure|May 11, 2022
Dynamic Ejection Fraction Trajectory in Patients With Dilated Cardiomyopathy With a Truncating Titin VariantMichiel T H M Henkens, Sophie L V M Stroeks, Anne G Raafs, et al.
Pageof 32

Showing results (131-140 of 318) with videos related to

Sort By:
Pageof 32
Human Genetics|April 17, 2007
Intragenic deletion in the LARGE gene causes Walker-Warburg syndromeJeroen van Reeuwijk, Prabhjit K Grewal, Mustafa A M Salih, et al.
Plos Genetics|November 9, 2013
Human intellectual disability genes form conserved functional modules in DrosophilaMerel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, et al.
European Journal of Pediatrics|October 17, 2014
Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadiasRomy van de Putte, Charlotte H W Wijers, Ivo de Blaauw, et al.
Nature Genetics|November 16, 2010
A de novo paradigm for mental retardationLisenka E L M Vissers, Joep de Ligt, Christian Gilissen, et al.
American Journal of Human Genetics|March 24, 2015
Absence of heterozygosity due to template switching during replicative rearrangementsClaudia M B Carvalho, Rolph Pfundt, Daniel A King, et al.
JACC. Heart Failure|August 28, 2023
Clonal Hematopoiesis Has Prognostic Value in Dilated Cardiomyopathy Independent of Age and Clone SizeMaurits A Sikking, Sophie L V M Stroeks, Michiel T H M Henkens, et al.
Journal of Medical Genetics|February 28, 2012
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defectsMarjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, et al.
Journal of Cardiac Failure|September 22, 2019
Metabolic Profiling Associates with Disease Severity in Nonischemic Dilated CardiomyopathyJob A J Verdonschot, Ping Wang, Marc Van Bilsen, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndromeNeil V Morgan, Louise A Brueton, Phillip Cox, et al.
Circulation. Heart Failure|May 11, 2022
Dynamic Ejection Fraction Trajectory in Patients With Dilated Cardiomyopathy With a Truncating Titin VariantMichiel T H M Henkens, Sophie L V M Stroeks, Anne G Raafs, et al.
Pageof 32