Associated Papers
Molecular diagnosis of 405 individuals with autism spectrum disorder.
Miyake N et al.
European Journal of Human Genetics : Ejhg, 2024
Case report: FOXP1 syndrome caused by a de novo splicing variant (c.1652+5 G>A) of the FOXP1 gene.
Chen M et al.
Frontiers in Genetics, 2022
Comprehensive Genetic Analysis of Non-syndromic Autism Spectrum Disorder in Clinical Settings.
Ohashi K et al.
Journal of Autism and Developmental Disorders, 2021
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