2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders
2p15-p16.1微缺失综合征:OTX1和XPO1基因的分子特征及其与自闭症谱系障碍的关联
期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/ejhg.2011.112
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 A