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Characterization of speech and language phenotype in children with NRXN1 deletions.

Pubmed ID: 
30358070
Year: 
2018
Month: 
Oct
Citation: 
Brignell A, St John M, Boys A, Bruce A, Dinale C, Pigdon L, Hildebrand MS, Amor DJ, Morgan AT. Characterization of speech and language phenotype in children with NRXN1 deletions. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (2018) PubMed (Grant IDs: 1063799, 1105008, 1116976)