Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35754/fullpdf
Reference28 articles.
1. Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication;Ballif;Mol Cytogenet,2008
2. Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia;Carroll;Am J Med Genet B Neuropsychiatr Genet,2011
3. Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder;Clayton-Smith;Clin Dysmorphol,2010
4. 1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child;Cobb;Eur J Med Genet,2010
5. Copy-number variations associated with neuropsychiatric conditions;Cook;Nature,2008
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