Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G Brunner

Showing results (461-470 of 727) with videos related to

Pageof 73
Sort By:
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.
Clinical Genetics|February 8, 2011
Intragenic deletion in DYRK1A leads to mental retardation and primary microcephalyB W M van Bon, A Hoischen, J Hehir-Kwa, 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.
Annals of Internal Medicine|December 1, 1979
Controlled trials of hemoperfusion for intoxicationO S Better, G Brunner, T M Chang, 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.
American Journal of Human Genetics|March 21, 2000
Familial syndromic esophageal atresia maps to 2p23-p24J Celli, E van Beusekom, R C Hennekam, 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 73

Showing results (461-470 of 727) with videos related to

Sort By:
Pageof 73
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.
Clinical Genetics|February 8, 2011
Intragenic deletion in DYRK1A leads to mental retardation and primary microcephalyB W M van Bon, A Hoischen, J Hehir-Kwa, 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.
Annals of Internal Medicine|December 1, 1979
Controlled trials of hemoperfusion for intoxicationO S Better, G Brunner, T M Chang, 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.
American Journal of Human Genetics|March 21, 2000
Familial syndromic esophageal atresia maps to 2p23-p24J Celli, E van Beusekom, R C Hennekam, 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 73