Cardiofaciocutaneous syndrome with rare structural variant in DOCK8 gene associated with neurodevelopmental disorders

gan Dell'Edera, Domenico, Debellis, Lucantonio, Mitidieri, Angela, Anna Epifania, Annunziata, Cuscianna, Eustachio, Allegretti, Arianna
Cyhoeddwyd yn Clin Case Rep (2020)