Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.

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Bibliographic Details
Title:	Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.
Authors:	Pettigrew KA; School of Medicine, University of St Andrews, St Andrews, United Kingdom., Reeves E; Department of Psychology, University of York, York, United Kingdom., Leavett R; Department of Psychology, University of York, York, United Kingdom., Hayiou-Thomas ME; Department of Psychology, University of York, York, United Kingdom., Sharma A; School of Medicine, University of St Andrews, St Andrews, United Kingdom., Simpson NH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom., Martinelli A; School of Medicine, University of St Andrews, St Andrews, United Kingdom., Thompson P; Department of Experimental Psychology, University of Oxford, Oxford, United Kingdom., Hulme C; Division of Psychology and Language Sciences, University College London, London, United Kingdom., Snowling MJ; Department of Experimental Psychology, University of Oxford, Oxford, United Kingdom; St. Johns College, University of Oxford, Oxford, United Kingdom., Newbury DF; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom., Paracchini S; School of Medicine, University of St Andrews, St Andrews, United Kingdom.
Source:	PloS one [PLoS One] 2015 Aug 11; Vol. 10 (8), pp. e0134997. Date of Electronic Publication: 2015 Aug 11 (Print Publication: 2015).
Publication Type:	Journal Article; Research Support, Non-U.S. Gov't
Journal Info:	Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	1932-6203
DOI:	10.1371/journal.pone.0134997