Associated Papers
De novo variants in PHF21A cause intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures: A case report and literature review.
Chen H et al.
Seizure, 2023
PHF21A Related Disorder: Description of a New Case.
Butera A et al.
International Journal of Molecular Sciences, 2022
Novel Pathogenic Variant (c.1171A>T) in PHF21A in a Female with Intellectual Disability and Craniofacial Anomalies.
Lee C et al.
Molecular Syndromology, 2022
De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomalies.
Hamanaka K et al.
European Journal of Human Genetics : Ejhg, 2019
Select a paper to view details