APA

Newbury D. F., Mari F., Sadighi Akha E., Macdermot K. D., Canitano R., Monaco A. P., Taylor J. C., Renieri A., Fisher S. E. & Knight S. J. L. (20130904). Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. : European journal of human genetics : EJHG.

Chicago

Newbury Dianne F, Mari Francesca, Sadighi Akha Elham, Macdermot Kay D, Canitano Roberto, Monaco Anthony P, Taylor Jenny C, Renieri Alessandra, Fisher Simon E and Knight Samantha J L. 20130904. Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. : European journal of human genetics : EJHG.

Harvard

Newbury D. F., Mari F., Sadighi Akha E., Macdermot K. D., Canitano R., Monaco A. P., Taylor J. C., Renieri A., Fisher S. E. and Knight S. J. L. (20130904). Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. : European journal of human genetics : EJHG.

MLA

Newbury Dianne F, Mari Francesca, Sadighi Akha Elham, Macdermot Kay D, Canitano Roberto, Monaco Anthony P, Taylor Jenny C, Renieri Alessandra, Fisher Simon E and Knight Samantha J L. Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. : European journal of human genetics : EJHG. 20130904.