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Showing results (21-30 of 31) with videos related to

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American Journal of Human Genetics|September 13, 2011
ST3GAL3 mutations impair the development of higher cognitive functionsHao Hu, Katinka Eggers, Wei Chen, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
Human Genetics|November 29, 2005
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephalyMasoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, et al.
Genome Research|March 11, 2008
Mapping translocation breakpoints by next-generation sequencingWei Chen, Vera Kalscheuer, Andreas Tzschach, et al.
Human Mutation|May 8, 2007
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardationReinhard Ullmann, Gillian Turner, Maria Kirchhoff, et al.
American Journal of Human Genetics|May 1, 2012
Mutations in NSUN2 cause autosomal-recessive intellectual disabilityLia Abbasi-Moheb, Sara Mertel, Melanie Gonsior, et al.
Plos Genetics|May 12, 2016
BOD1 Is Required for Cognitive Function in Humans and DrosophilaSahar Esmaeeli-Nieh, Michaela Fenckova, Iain M Porter, et al.
American Journal of Human Genetics|December 17, 2009
Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardationAsif Mir, Liana Kaufman, Abdul Noor, et al.
Human Genetics|November 23, 2006
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene lociHossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, et al.
European Journal of Human Genetics : EJHG|February 26, 2015
Intelligence: shared genetic basis between Mendelian disorders and a polygenic traitSanja Franić, Maria M Groen-Blokhuis, Conor V Dolan, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|September 13, 2011
ST3GAL3 mutations impair the development of higher cognitive functionsHao Hu, Katinka Eggers, Wei Chen, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
Human Genetics|November 29, 2005
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephalyMasoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, et al.
Genome Research|March 11, 2008
Mapping translocation breakpoints by next-generation sequencingWei Chen, Vera Kalscheuer, Andreas Tzschach, et al.
Human Mutation|May 8, 2007
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardationReinhard Ullmann, Gillian Turner, Maria Kirchhoff, et al.
American Journal of Human Genetics|May 1, 2012
Mutations in NSUN2 cause autosomal-recessive intellectual disabilityLia Abbasi-Moheb, Sara Mertel, Melanie Gonsior, et al.
Plos Genetics|May 12, 2016
BOD1 Is Required for Cognitive Function in Humans and DrosophilaSahar Esmaeeli-Nieh, Michaela Fenckova, Iain M Porter, et al.
American Journal of Human Genetics|December 17, 2009
Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardationAsif Mir, Liana Kaufman, Abdul Noor, et al.
Human Genetics|November 23, 2006
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene lociHossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, et al.
European Journal of Human Genetics : EJHG|February 26, 2015
Intelligence: shared genetic basis between Mendelian disorders and a polygenic traitSanja Franić, Maria M Groen-Blokhuis, Conor V Dolan, et al.
Pageof 4