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Showing results (701-710 of 719) with videos related to

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American Journal of Human Genetics|August 4, 2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairmentDianne F Newbury, Laura Winchester, Laura Addis, et al.
European Journal of Human Genetics : EJHG|November 4, 2004
Mutation screening and association analysis of six candidate genes for autism on chromosome 7qElena Bonora, Janine A Lamb, Gabrielle Barnby, et al.
European Journal of Human Genetics : EJHG|September 12, 2013
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohortJessica Becker, Darina Czamara, Tom S Scerri, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosisC Dobson-Stone, A Danek, L Rampoldi, et al.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Translational Psychiatry|February 12, 2019
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Molecular Psychiatry|October 15, 2020
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, et al.
Pageof 72

Showing results (701-710 of 719) with videos related to

Sort By:
Pageof 72
American Journal of Human Genetics|August 4, 2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairmentDianne F Newbury, Laura Winchester, Laura Addis, et al.
European Journal of Human Genetics : EJHG|November 4, 2004
Mutation screening and association analysis of six candidate genes for autism on chromosome 7qElena Bonora, Janine A Lamb, Gabrielle Barnby, et al.
European Journal of Human Genetics : EJHG|September 12, 2013
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohortJessica Becker, Darina Czamara, Tom S Scerri, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosisC Dobson-Stone, A Danek, L Rampoldi, et al.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Translational Psychiatry|February 12, 2019
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Molecular Psychiatry|October 15, 2020
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, et al.
Pageof 72