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Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.
PLoS One. 2015 Aug 11;10(8):e0134997. doi: 10.1371/journal.pone.0134997. eCollection 2015.
PLoS One. 2015.
PMID: 26262844
Free PMC article.
Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Simpson NH, Ceroni F, Reader RH, Covill LE, Knight JC; SLI Consortium; Hennessy ER, Bolton PF, Conti-Ramsden G, O'Hare A, Baird G, Fisher SE, Newbury DF.
Simpson NH, et al.
Eur J Hum Genet. 2015 Oct;23(10):1370-7. doi: 10.1038/ejhg.2014.296. Epub 2015 Jan 14.
Eur J Hum Genet. 2015.
PMID: 25585696
Free PMC article.
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