The Cognitive and Behavioral Phenotype of the 16p11.2 Deletion in a Clinically Ascertained Population-Reference-Cited by-同舟云学术

The Cognitive and Behavioral Phenotype of the 16p11.2 Deletion in a Clinically Ascertained Population

Published:2015-05 Issue:9 Volume:77 Page:785-793
ISSN:0006-3223
Container-title:Biological Psychiatry
language:en
Short-container-title:Biological Psychiatry

Author:

Hanson Ellen^ORCID,Bernier Raphael,Porche Ken,Jackson Frank I.,Goin-Kochel Robin P.,Snyder LeeAnne Green,Snow Anne V.,Wallace Arianne Stevens,Campe Katherine L.,Zhang Yuan^ORCID,Chen Qixuan,D’Angelo Debra,Moreno-De-Luca Andres,Orr Patrick T.,Boomer K.B.,Evans David W.,Kanne Stephen,Berry Leandra,Miller Fiona K.,Olson Jennifer,Sherr Elliot,Martin Christa L.,Ledbetter David H.,Spiro John E.,Chung Wendy K.

Funder

Simons Foundation

WKC and Simons Foundation Autism Research Initiative

National Institutes of Health

Publisher

Elsevier BV

Subject

Biological Psychiatry

Reference58 articles.

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2. Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications;Rosenfeld;J Neurodev Disord,2010

3. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size;Shinawi;J Med Genet,2010