Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Mental Retardation and NRXN1[original query] |
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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Jun 153B (4): 937-47. Ching Michael S L, Shen Yiping, Tan Wen-Hann, Jeste Shafali S, Morrow Eric M, Chen Xiaoli, Mukaddes Nahit M, Yoo Seung-Yun, Hanson Ellen, Hundley Rachel, Austin Christina, Becker Ronald E, Berry Gerard T, Driscoll Katherine, Engle Elizabeth C, Friedman Sandra, Gusella James F, Hisama Fuki M, Irons Mira B, Lafiosca Tina, LeClair Elaine, Miller David T, Neessen Michael, Picker Jonathan D, Rappaport Leonard, Rooney Cynthia M, Sarco Dean P, Stoler Joan M, Walsh Christopher A, Wolff Robert R, Zhang Ting, Nasir Ramzi H, Wu Bai-Lin, |
Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. The American journal of psychiatry 2011 Mar 168 (3): 302-16. Levinson Douglas F, Duan Jubao, Oh Sang, Wang Kai, Sanders Alan R, Shi Jianxin, Zhang Nancy, Mowry Bryan J, Olincy Ann, Amin Farooq, Cloninger C Robert, Silverman Jeremy M, Buccola Nancy G, Byerley William F, Black Donald W, Kendler Kenneth S, Freedman Robert, Dudbridge Frank, Pe'er Itsik, Hakonarson Hakon, Bergen Sarah E, Fanous Ayman H, Holmans Peter A, Gejman Pablo |
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- Page last updated:Apr 29, 2024
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