Dual copy number variants involving 16p11 and 6q22 in a...

European Journal of Human Genetics 2013 / 4 Vol. 21; Iss. 4

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder

Newbury, Dianne F, Mari, Francesca, Sadighi Akha, Elham, MacDermot, Kay D, Canitano, Roberto, Monaco, Anthony P, Taylor, Jenny C, Renieri, Alessandra, Fisher, Simon E, Knight, Samantha J L
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Volume:
21
Language:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2012.166
Date:
April, 2013
File:
PDF, 707 KB
english, 2013
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