Cite
HARVARD Citation
Turner, S. et al. (n.d.). Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria. American journal of medical genetics. 161 (9), pp. 2321-2326. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Turner, S. et al. (n.d.). Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria. American journal of medical genetics. 161 (9), pp. 2321-2326. [Online].