Unmasking a novel disease gene NEO1 associated with autism spectrum disorders by a hemizygous deletion on chromosome 15 and a functional polymorphism
Author:
Publisher
Elsevier BV
Subject
Behavioral Neuroscience
Reference63 articles.
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2. Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting;Betancur;Brain Res.,2011
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4. A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region;McInnes;Mol. Autism,2010
5. Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3Mb in a patient with Wolf-Hirschhorn syndrome;Flipsen-ten Berg;Eur. J. Hum. Genet.,2007
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