Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders-Reference-Cited by-同舟云学术

Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders

Published:2016-08-26 Issue:8 Volume:171 Page:1088-1098
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Picinelli Chiara¹²,Lintas Carla¹,Piras Ignazio Stefano¹²,Gabriele Stefano¹,Sacco Roberto¹,Brogna Claudia¹,Persico Antonio Maria²³

Affiliation:

1. Unit of Child and Adolescent NeuroPsychiatry & Laboratory of Molecular Psychiatry and Neurogenetics; University “Campus Bio-Medico”; Rome Italy

2. Mafalda Luce Center for Pervasive Developmental Disorders; Milan Italy

3. Unit of Child and Adolescent Neuropsychiatry, “Gaetano Martino” University Hospital; University of Messina; Messina Italy

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Reference61 articles.

2. Individual common variants exert weak effects on the risk for autism spectrum disorderspi;Anney;Hum Mol Genet

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