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A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.

Pubmed ID: 
26763793
Year: 
2016
Month: 
Feb
Volume: 
24
Issue: 
2
Citation: 
Fedorenko E, Morgan A, Murray E, Cardinaux A, Mei C, Tager-Flusberg H, Fisher SE, Kanwisher N. A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2. European journal of human genetics : EJHG 24 (2) : 310(2016) PubMed