Association studies of theHOPA dodecamer duplication variant in different subtypes of autism
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference30 articles.
1. Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families
2. An autosomal genomic screen for autism
3. A Case-Control Family History Study of Autism
4. Analysis of canonical and non-canonical splice sites in mammalian genomes
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2. A case report of two male siblings with autism and duplication of Xq13–q21, a region including three genes predisposing for autism;European Child & Adolescent Psychiatry;2013-08-23
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4. Effects of Bisphenol-A and Other Endocrine Disruptors Compared With Abnormalities of Schizophrenia: An Endocrine-Disruption Theory of Schizophrenia;Schizophrenia Bulletin;2009-01-01
5. Role of MED12 in transcription and human behavior;Pharmacogenomics;2007-08
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