Macrocephaly as a Clinical Indicator of Genetic Subtypes in Autism
Author:
Affiliation:
1. Department of Human Genetics; David Geffen School of Medicine at UCLA; Los Angeles; California
2. Division of Pediatric Neurology; David Geffen School of Medicine at UCLA; Los Angeles; California
Publisher
Wiley
Subject
Genetics(clinical),Clinical Neurology,General Neuroscience
Reference31 articles.
1. Dissecting the clinical heterogeneity of autism spectrum disorders through defined genotypes;Bruining;PLoS ONE,2010
2. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities;Brunetti-Pierri;Nature Genetics,2008
3. Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations;Butler;Journal of Medical Genetics,2005
4. Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly;Buxbaum;American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics,2007
5. Mental deficiency, alterations in performance, and CNS abnormalities in overgrowth syndromes;Cohen;American Journal of Medical Genetics. Part C, Seminars in Medical Genetics,2003
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