Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders-Reference-Cited by-同舟云学术

Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders

Published:2012-10-03 Issue:6 Volume:21 Page:620-625
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Wiśniowiecka-Kowalnik Barbara,Kastory-Bronowska Monika,Bartnik Magdalena,Derwińska Katarzyna,Dymczak-Domini Wanda,Szumbarska Dorota,Ziemka Ewa,Szczałuba Krzysztof,Sykulski Maciej,Gambin Tomasz,Gambin Anna,Shaw Chad A,Mazurczak Tadeusz,Obersztyn Ewa,Bocian Ewa,Stankiewicz Paweł

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2012219.pdf

Reference37 articles.

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2. Cusco I, Medrano A, Gener B et al: Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder. Hum Mol Genet 2009; 18: 1795–1804.

3. Glessner JT, Wang K, Cai G et al: Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 2009; 459: 569–573.

4. Pinto D, Pagnamenta AT, Klei L et al: Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010; 466: 368–372.

5. Betancur C : Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. Brain Res 2011; 1380: 42–77.

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