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Abnormal auditory and language pathways in children with 16p11.2 deletion
Published Web Location
http://europepmc.org/articles/PMC4543079?pdf=renderNo data is associated with this publication.
Abstract
© 2015 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license.Copy number variations at chromosome 16p11.2 contribute to neurodevelopmental disorders, including autism spectrum disorder (ASD). This study seeks
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