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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: May 30, 2023. (Total: 217422Documents)
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Query Trace: Syndrome and OTX1[original query]
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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