Publications:

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

European Journal Of Human Genetics : Ejhg

Liu, Xudong X; Malenfant, Patrick P; Reesor, Chelsea C; Lee, Alana A; Hudson, Melissa L ML; Harvard, Chansonette C; Qiao, Ying Y; Persico, Antonio M AM; Cohen, Ira L IL; Chudley, Albert E AE; Forster-Gibson, Cynthia C; Rajcan-Separovic, Evica E; Lewis, M E Suzanne ME; Holden, Jeanette J A JJ

Publication Date: 2011-12

Variant appearance in text: rs7563678

PubMed Link: 21750575

Variant Present in the following documents:

• Main text

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