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

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Publisher copy:
10.1038/ejhg.2012.166

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Journal:
European Journal of Human Genetics
Volume:
21
Issue:
4
Pages:
361-365
Publication date:
2013-04-01
DOI:
EISSN:
1476-5438
ISSN:
1018-4813
Source identifiers:
394113
Language:
English
Pubs id:
pubs:394113
UUID:
uuid:caecb905-4144-4171-b29d-8c61bc64741c
Local pid:
pubs:394113
Deposit date:
2013-11-16

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