Associated Papers
Clinical utility of genome sequencing in autism: illustrative examples from a genomic research study.
Selvanayagam T et al.
Journal of Medical Genetics, 2025
Clinical features of CNOT3-associated neurodevelopmental disorder in three Chinese patients.
Zhao P et al.
Neurogenetics, 2023
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_
De novo variants in CNOT3 cause a variable neurodevelopmental disorder.
Martin R et al.
European Journal of Human Genetics : Ejhg, 2019
Select a paper to view details