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Showing results (21-30 of 26) with videos related to

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European Journal of Human Genetics : EJHG|June 16, 2019
De novo variants in CNOT3 cause a variable neurodevelopmental disorderR Martin, M Splitt, D Genevieve, et al.
Translational Psychiatry|July 27, 2012
Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophreniaJ Tarabeux, O Kebir, J Gauthier, et al.
BMC Health Services Research|April 21, 2023
Cost of exome analysis in patients with intellectual disability: a micro-costing study in a French settingA L Soilly, C Robert-Viard, C Besse, et al.
Molecular Psychiatry|May 19, 2010
Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophreniaA Piton, J Gauthier, F F Hamdan, et al.
Clinical Genetics|March 26, 2018
Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French casesS Baer, A Afenjar, T Smol, et al.
Neurogenetics|March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotypeT Smol, F Petit, A Piton, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
European Journal of Human Genetics : EJHG|June 16, 2019
De novo variants in CNOT3 cause a variable neurodevelopmental disorderR Martin, M Splitt, D Genevieve, et al.
Translational Psychiatry|July 27, 2012
Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophreniaJ Tarabeux, O Kebir, J Gauthier, et al.
BMC Health Services Research|April 21, 2023
Cost of exome analysis in patients with intellectual disability: a micro-costing study in a French settingA L Soilly, C Robert-Viard, C Besse, et al.
Molecular Psychiatry|May 19, 2010
Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophreniaA Piton, J Gauthier, F F Hamdan, et al.
Clinical Genetics|March 26, 2018
Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French casesS Baer, A Afenjar, T Smol, et al.
Neurogenetics|March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotypeT Smol, F Petit, A Piton, et al.
Pageof 3