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

Newbury, Df F.; Mari, Francesca; Akha, Elham Sadighi; Sadighi Akha, Elham; Macdermot, Kd D.; Canitano, Roberto; Monaco, Ap P.; Taylor, Jc C.; Renieri, Alessandra; Fisher, Se E.; Knight, Sj J. L.

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

Journal article published in 2012 by Df F. Newbury, Francesca Mari, Elham Sadighi Akha, Elham Sadighi Akha, Kd D. Macdermot, Roberto Canitano, Ap P. Monaco, Jc C. Taylor

, Alessandra Renieri, Se E. Fisher

, Sj J. L. Knight

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Abstract

The European Journal of Human Genetics is the official Journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports, News and Commentary articles and reviews in the rapidly expanding field of human genetics and genomics.

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

Abstract