Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.

Source:http://linkedlifedata.com/resource/pubmed/id/17330859

Am. J. Med. Genet. A 2007 Apr 15 143A 8 791-8

Download in:

View as

Triples

General Info

PMID
17330859