Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

R. W. Davies, Ania Fiksinski, Elemi Breetvelt, Nigel Williams, Stephen R. Hooper, Thomas Monfeuga, Anne S. Bassett, Michael J. Owen, Raquel E. Gur, Bernice E. Morrow,

Nature Medicine · 2020 · 149 citations · 46 references

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