Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH-Reference-Cited by-同舟云学术

Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH

Published:2014-01 Issue:1 Volume:46 Page:41-45
ISSN:0031-3025
Container-title:Pathology
language:en
Short-container-title:Pathology

Author:

Nicholl Jillian,Waters Wendy,Mulley John C.,Suwalski Shanna,Brown Sue,Hull Yvonne,Barnett Christopher,Haan Eric,Thompson Elizabeth M.,Liebelt Jan,Mcgregor Lesley,Harbord Michael G.,Entwistle John,Munt Chris,White Dierdre,Chitti Anthony,Baulderstone David,Ketteridge David,Friend Kathryn,Bain Sharon M.,Sui Y.u.

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference37 articles.

1. A recurrent 15ql3.3 microdeletion syndrome associated with mental retardation and seizures;Sharp;Nat Genet,2008

2. Array CGH in patients with learning disability (mental retardation) and congenital abnormalities: an updated systematic review and meta-analysis of 19 studies and 13,926 subjects;Sagoo;Genet Med,2009

3. Recurrent microdeletions at 15ql 1.2 and 16pl3.11 predispose to idiopathic generalized epilepsies;de Kovel;Brain,2010

4. A recurrent 16pl2.1 micro-deletion supports a two-hit model for severe developmental delay;Girirajan;Nat Genet,2010

5. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies;Miller;Am J Hum Genet,2010

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