Identification of single gene deletions at 15q13.3: further evidence thatCHRNA7causes the 15q13.3 microdeletion syndrome phenotype
Author:
Affiliation:
1. Department of Laboratory Medicine and Pathology; Mayo Clinic; Rochester; MN; USA
2. Genetic Services; Our Lady of the Lake Regional Medical Center; Baton Rouge; LA; USA
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2012.01925.x/fullpdf
Reference20 articles.
1. Rare chromosomal deletions and duplications increase risk of schizophrenia;International Schizophrenia Consortium;Nature,2008
2. Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders;Ben-Shachar;J Med Genet,2009
3. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders;Miller;J Med Genet,2009
4. A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures;Sharp;Nat Genet,2008
5. Large recurrent microdeletions associated with schizophrenia;Stefansson;Nature,2008
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