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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome by Davies, RW, Fiksinski, AM, Breetvelt, EJ, Williams, NM, Hooper, SR, Monfeuga, T, Bassett, AS, Owen, MJ, Gur, RE, Morrow, BE, McDonald-McGinn, DM, Swillen, A, Chow, EWC, van den Bree, M, Emanuel, BS, Vermeesch, JR, van Amelsvoort, T, Arango, C, Armando, M, Campbell, LE, Cubells, JF, Eliez, S, Garcia-Minaur, S, Gothelf, D, Kates, WR, Murphy, KC, Murphy, CM, Murphy, DG, Philip, N, Repetto, GM, Shashi, V, Simon, TJ, Suñer, DH, Vicari, S, Scherer, SW, Bearden, CE, Vorstman, JAS, International 22q11.2 Brain and Behavior Consortium
Published 2020Journal article