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Han G Brunner

Showing results (101-110 of 318) with videos related to

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Human Reproduction (Oxford, England)|September 25, 2021
Liquid biopsy: state of reproductive medicine and beyondGaby Schobers, Rebekka Koeck, Dominique Pellaers, et al.
Human Mutation|July 30, 2013
Detection of clinically relevant copy number variants with whole-exome sequencingJoep de Ligt, Philip M Boone, Rolph Pfundt, et al.
JIMD Reports|March 17, 2021
Monoamine oxidase A activity in fibroblasts as a functional confirmation of <i>MAOA</i> variantsTessa M A Peters, Irma Lammerts van Bueren, Ben P B H Geurtz, et al.
Nucleic Acids Research|June 8, 2006
Computational disease gene identification: a concert of methods prioritizes type 2 diabetes and obesity candidate genesNicki Tiffin, Euan Adie, Frances Turner, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|August 17, 2010
Heritability of head size in Dutch and Australian twin families at ages 0-50 yearsDirk J A Smit, Michelle Luciano, Meike Bartels, et al.
American Journal of Human Genetics|September 7, 2010
Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndromeChristian Gilissen, Heleen H Arts, Alexander Hoischen, et al.
Human Mutation|December 17, 2008
Genomic microarrays in mental retardation: a practical workflow for diagnostic applicationsDavid A Koolen, Rolph Pfundt, Nicole de Leeuw, et al.
American Journal of Human Genetics|December 14, 2011
Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humansIlse Feenstra, Lisenka E L M Vissers, Ronald J E Pennings, et al.
American Journal of Medical Genetics. Part A|December 13, 2007
Familial CHARGE syndrome and the CHD7 gene: a recurrent missense mutation, intrafamilial recurrence and variabilityMarjolijn C J Jongmans, Lies H Hoefsloot, Kim P van der Donk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2012
Alu elements mediate large SPG11 gene rearrangements: further spatacsin mutationsMaria Conceição Pereira, José Leal Loureiro, Jorge Pinto-Basto, et al.
Pageof 32

Showing results (101-110 of 318) with videos related to

Sort By:
Pageof 32
Human Reproduction (Oxford, England)|September 25, 2021
Liquid biopsy: state of reproductive medicine and beyondGaby Schobers, Rebekka Koeck, Dominique Pellaers, et al.
Human Mutation|July 30, 2013
Detection of clinically relevant copy number variants with whole-exome sequencingJoep de Ligt, Philip M Boone, Rolph Pfundt, et al.
JIMD Reports|March 17, 2021
Monoamine oxidase A activity in fibroblasts as a functional confirmation of <i>MAOA</i> variantsTessa M A Peters, Irma Lammerts van Bueren, Ben P B H Geurtz, et al.
Nucleic Acids Research|June 8, 2006
Computational disease gene identification: a concert of methods prioritizes type 2 diabetes and obesity candidate genesNicki Tiffin, Euan Adie, Frances Turner, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|August 17, 2010
Heritability of head size in Dutch and Australian twin families at ages 0-50 yearsDirk J A Smit, Michelle Luciano, Meike Bartels, et al.
American Journal of Human Genetics|September 7, 2010
Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndromeChristian Gilissen, Heleen H Arts, Alexander Hoischen, et al.
Human Mutation|December 17, 2008
Genomic microarrays in mental retardation: a practical workflow for diagnostic applicationsDavid A Koolen, Rolph Pfundt, Nicole de Leeuw, et al.
American Journal of Human Genetics|December 14, 2011
Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humansIlse Feenstra, Lisenka E L M Vissers, Ronald J E Pennings, et al.
American Journal of Medical Genetics. Part A|December 13, 2007
Familial CHARGE syndrome and the CHD7 gene: a recurrent missense mutation, intrafamilial recurrence and variabilityMarjolijn C J Jongmans, Lies H Hoefsloot, Kim P van der Donk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2012
Alu elements mediate large SPG11 gene rearrangements: further spatacsin mutationsMaria Conceição Pereira, José Leal Loureiro, Jorge Pinto-Basto, et al.
Pageof 32