NovelPTENmutations in neurodevelopmental disorders and macrocephaly
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2008.01074.x/fullpdf
Reference17 articles.
1. Childhood autism and associated comorbidities;Zafeiriou;Brain Dev,2007
2. PTEN mutation in a family with Cowden syndrome and autism;Goffin;Am J Med Genet,2001
3. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome;Marsh;Hum Mol Genet,1999
4. Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes;Pezzolesi;Am J Hum Genet,2006
5. Increasing knowledge of PTEN germline mutations: Two additional patients with autism and macrocephaly;Butler;Am J Med Genet A,2007
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