Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
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| Description | scientific article published on 09 November 2020 |
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author: Joris R Vermeesch Stephen R. Hooper Stephen W. Scherer Anne S Bassett Ann Swillen Stephan Eliez Ania Fiksinski Linda E Campbell Jacob A S Vorstman Donna M McDonald-McGinn Carrie E Bearden Wendy R Kates Thérèse A.M.J. Van Amelsvoort Robert W Davies Celso Arango Michael Owen Declan Murphy |
| Publication date | November 9, 2020 |
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