Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
ContributorsDavies, Robert W; Fiksinski, Ania M; Breetvelt, Elemi J; Williams, Nigel M; Hooper, Stephen R; Monfeuga, Thomas; Bassett, Anne S; Owen, Michael J; Gur, Raquel E; Morrow, Bernice E; McDonald-McGinn, Donna M; Swillen, Ann; Chow, Eva W C; van den Bree, Marianne; Emanuel, Beverly S; Vermeesch, Joris R; van Amelsvoort, Therese; Arango, Celso; Armando, Marco; Campbell, Linda E; Cubells, Joseph F; Eliez, Stéphan; Garcia-Minaur, Sixto; Gothelf, Doron; Kates, Wendy R; Murphy, Kieran C; Murphy, Clodagh M; Murphy, Declan G; Philip, Nicole; Repetto, Gabriela M; Shashi, Vandana; Simon, Tony J; Suñer, Damiàn Heine; Vicari, Stefano; Scherer, Stephen W; Bearden, Carrie E; Vorstman, Jacob A S; International 22q11.2 Brain and Behavior Consortium
Published inNature Medicine, vol. 26, no. 12, p. 1912-1918
Publication date2020
Abstract
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Citation (ISO format)
DAVIES, Robert W et al. Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. In: Nature Medicine, 2020, vol. 26, n° 12, p. 1912–1918. doi: 10.1038/s41591-020-1103-1
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- PID : unige:148764
- DOI : 10.1038/s41591-020-1103-1
- PMID : 33169016
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Journal ISSN1078-8956