Human Genome Epidemiology Literature Finder
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Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular psychiatry 2023 3 . Lin Jhih-Rong, Zhao Yingjie, Jabalameli M Reza, Nguyen Nha, Mitra Joydeep, , Swillen Ann, Vorstman Jacob A S, Chow Eva W C, van den Bree Marianne, Emanuel Beverly S, Vermeesch Joris R, Owen Michael J, Williams Nigel M, Bassett Anne S, McDonald-McGinn Donna M, Gur Raquel E, Bearden Carrie E, Morrow Bernice E, Lachman Herbert M, Zhang Zhengdong |
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