HuGE Literature Finder
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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 2011 Dec 19 (12): 1264-70. 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 M E Suzanne, Holden Jeanette J |
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