Associated Papers
Autism-like features and FOXP1 syndrome: A scoping review.
Stewart J et al.
Brain & Development, 2025
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals.
Koene S et al.
Journal of Medical Genetics, 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
A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome.
Urreizti R et al.
Scientific Reports, 2018
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