2p15–p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders-Reference-Cited by-同舟云学术

2p15–p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

Published:2011-07-13 Issue:12 Volume:19 Page:1264-1270
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Liu Xudong,Malenfant Patrick,Reesor Chelsea,Lee Alana,Hudson Melissa L,Harvard Chansonette,Qiao Ying,Persico Antonio M,Cohen Ira L,Chudley Albert E,Forster-Gibson Cynthia,Rajcan-Separovic Evica,Lewis ME Suzanne,Holden Jeanette JA

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2011112.pdf

Reference54 articles.

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3. Miles JH, Takahashi TN, Bagby S et al: Essential versus complex autism: definition of fundamental prognostic subtypes. Am J Med Genet A 2005; 135: 171–180.

4. Gillberg C : Chromosomal disorders and autism. J Autism Dev Disord 1998; 28: 415–425.

5. Cook Jr EH, Lindgren V, Leventhal BL et al: Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet 1997; 60: 928–934.

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