3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients
Author:
Affiliation:
1. Unit of Psychology; IRCCS Associazione Oasi Maria Santissima; Troina Italy
2. Unit of Pediatrics and Medical Genetics; IRCCS Associazione Oasi Maria Santissima; Troina Italy
3. Fondazione IRCCS Istituto Neurologico Carlo Besta; Milano Italy
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36142/fullpdf
Reference31 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 Part B,2011
3. Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder;Clayton-Smith;Clin Dysmorphol,2010
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