16p11.2 Copy Number Variations and Neurodevelopmental Disorders
Author:
Funder
Nancy Lurie Marks Family Foundation
National Institutes of Health
Publisher
Elsevier BV
Subject
General Neuroscience
Reference103 articles.
1. The genetics of neurodevelopmental disease;Mitchell;Curr. Opin. Neurobiol.,2011
2. Copy number variations in neurodevelopmental disorders;Grayton;Prog. Neurobiol.,2012
3. Global variation in copy number in the human genome;Redon;Nature,2006
4. Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome;Portmann;Cell Rep.,2014
5. Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism;Horev;PNAS,2011
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