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Dive into the research topics of 'Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome'. Together they form a unique fingerprint.- Sort by
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Anne S. Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W.C. Chow, Therese Van Amelsvoort, Donna McDonald-McGinn, Raquel E. Gur, Ann Swillen, Marianne Van Den Bree, Kieran Murphy, Doron Gothelf, Carrie E. Bearden, Stephan Eliez, Wendy Kates, Nicole Philip, Vandana Sashi, Linda Campbell, Jacob Vorstman, Joseph Cubells
Research output: Contribution to journal › Article › peer-review