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

Autor: Jeffrey I. Berman, Darina Chudnovskaya, Lisa Blaskey, Emily Kuschner, Pratik Mukherjee, Randall Buckner, Srikantan Nagarajan, Wendy K. Chung, John E. Spiro, Elliott H. Sherr, Timothy P.L. Roberts

Publikováno v: NeuroImage: Clinical, Vol 9, Iss C, Pp 50-57 (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 common in ASD, in partic

Externí odkaz: https://doaj.org/article/91d23987d96f4e11b3868cb75cdc3ba1

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

Autor: Emily S. Kuschner, Elliott H. Sherr, Randall Buckner, Jeffrey I. Berman, Darina Chudnovskaya, Wendy K. Chung, Srikantan S. Nagarajan, John E. Spiro, Timothy P.L. Roberts, Lisa Blaskey, Pratik Mukherjee

Publikováno v: Sherr, Elliott; Mukherjee, Pratik; Berman, JI; Chudnovskaya, D; Blaskey, L; Kuschner, E; et al.(2015). Abnormal auditory and language pathways in children with 16p11.2 deletion. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/44p5t5dn
NeuroImage: Clinical, Vol 9, Iss C, Pp 50-57 (2015)
NeuroImage : Clinical

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 common in ASD, in partic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24fa27b0c755e32733dee936a882bf15
http://www.escholarship.org/uc/item/44p5t5dn