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Fabien Fauchereau

Showing results (21-30 of 24) with videos related to

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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.
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.
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Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
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.
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.
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