Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome-Reference-Cited by-同舟云学术

Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome

Published:2009-11-18 Issue:4 Volume:18 Page:429-435
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Willemsen Marjolein H,Fernandez Bridget A,Bacino Carlos A,Gerkes Erica,de Brouwer Arjan PM,Pfundt Rolph,Sikkema-Raddatz Birgit,Scherer Stephen W,Marshall Christian R,Potocki Lorraine,van Bokhoven Hans,Kleefstra Tjitske

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2009192.pdf

Reference45 articles.

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4. Friedman JM, Baross A, Delaney AD et al: Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation. Am J Hum Genet 2006; 79: 500–513.

5. Koolen DA, Sharp AJ, Hurst JA et al: Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. J Med Genet 2008; 45: 710–720.

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