Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment.
Palka C, Alfonsi M, Mohn A, Cerbo R, Guanciali Franchi P, Fantasia D, Morizio E, Stuppia L, Calabrese G, Zori R, Chiarelli F, Palka G.
Palka C, et al. Among authors: chiarelli f.
Pediatrics. 2012 Jan;129(1):e183-8. doi: 10.1542/peds.2010-2094. Epub 2011 Dec 5.
Pediatrics. 2012.
PMID: 22144704