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Abnormal auditory and language pathways in children with 16p11.2 deletion

  • Author(s): Sherr, Elliott
  • Mukherjee, Pratik
  • Berman, JI
  • Chudnovskaya, D
  • Blaskey, L
  • Kuschner, E
  • Buckner, R
  • Nagarajan, S
  • Chung, WK
  • Spiro, JE
  • Sherr, EH
  • et al.

Published Web Location

http://europepmc.org/articles/PMC4543079?pdf=render
No 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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