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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
Davies, 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-MJournal:
Nature Medicine
DOI:
10.1038/s41591-020-1103-1
Date:
November, 2020
File:
PDF, 1.63 MB
2020