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

• Kerry A. Pettigrew,

  Affiliation School of Medicine, University of St Andrews, St Andrews, United Kingdom

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• Emily Reeves,

  Affiliation Department of Psychology, University of York, York, United Kingdom

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• Ruth Leavett,

  Affiliation Department of Psychology, University of York, York, United Kingdom

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• Marianna E. Hayiou-Thomas,

  Affiliation Department of Psychology, University of York, York, United Kingdom

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• Anahita Sharma,

  Affiliation School of Medicine, University of St Andrews, St Andrews, United Kingdom

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• Nuala H. Simpson,

  Affiliation Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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• Angela Martinelli,

  Affiliation School of Medicine, University of St Andrews, St Andrews, United Kingdom

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• Paul Thompson,

  Affiliation Department of Experimental Psychology, University of Oxford, Oxford, United Kingdom

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• Charles Hulme,

  Affiliation Division of Psychology and Language Sciences, University College London, London, United Kingdom

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• Margaret J. Snowling,

  Affiliations Department of Experimental Psychology, University of Oxford, Oxford, United Kingdom, St. Johns College, University of Oxford, Oxford, United Kingdom

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• Dianne F. Newbury,

  Affiliation Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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• Silvia Paracchini

  * E-mail: sp58@st-andrews.ac.uk

  Affiliation School of Medicine, University of St Andrews, St Andrews, United Kingdom

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