Author:
Duyzend Michael H.,Nuttle Xander,Coe Bradley P.,Baker Carl,Nickerson Deborah A.,Bernier Raphael,Eichler Evan E.
Funder
US National Institute of Mental Health
Simons Foundation
US National Science Foundation
Simons Foundation Autism Research Initiative
NIH
Subject
Genetics(clinical),Genetics
Reference57 articles.
1. Association between microdeletion and microduplication at 16p11.2 and autism;Weiss;N. Engl. J. Med.,2008
2. Recurrent 16p11.2 microdeletions in autism;Kumar;Hum. Mol. Genet.,2008
3. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size;Shinawi;J. Med. Genet.,2010
4. 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
5. The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions;Moreno-De-Luca;JAMA Psychiatry,2015
Cited by
53 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献