Associated Papers
Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.
Engel C et al.
European Journal of Human Genetics : Ejhg, 2025
Clinical utility of genome sequencing in autism: illustrative examples from a genomic research study.
Selvanayagam T et al.
Journal of Medical Genetics, 2025
Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.
Zhang Y et al.
Molecular Neurobiology, 2021
33860439 (PubMed )
Supplement: 12035_2021_2377_MOESM14_ESM.xlsx › NDD_probands__public_
Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use.
Husson T et al.
Translational Psychiatry, 2020
32094338 (PubMed )
Supplement: 41398_2020_760_MOESM2_ESM.xlsx › De_novo
De novo variants in CNOT3 cause a variable neurodevelopmental disorder.
Martin R et al.
European Journal of Human Genetics : Ejhg, 2019
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