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

      Berman, Jeffrey I.; Chudnovskaya, Darina; Blaskey, Lisa; Kuschner, Emily; Mukherjee, Pratik; Buckner, Randall; Nagarajan, Srikantan; Chung, Wendy K.; Spiro, John E.; Sherr, Elliott H.; Roberts, Timothy P.L. (Elsevier, 2015)
      Copy number variations at chromosome 16p11.2 contribute to neurodevelopmental disorders, including autism spectrum disorder (ASD). This study seeks to improve our understanding of the biological basis of behavioral phenotypes ...