Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome - Robert W. Davies, Nigel M. Williams, Stephen R. Hooper, Thomas Monfeuga, Michael J. Owen, Bernice E. Morrow, Donna M. McDonald-Mcginn, Ann Swillen, Marianne van den Bree, Joris R. Vermeesch, Therese van Amelsvoort, S. T. Warren, Wendy R. Kates, S. Morrison, Kieran C. Murphy - Dissemin

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Nature Research, Nature Medicine, 12(26), p. 1912-1918, 2020

DOI: 10.1038/s41591-020-1103-1

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

Journal article published in 2020 by Robert W. Davies, Nigel M. Williams, Stephen R. Hooper, Thomas Monfeuga, Michael J. Owen, Bernice E. Morrow, Donna M. McDonald-Mcginn, Ann Swillen, Marianne van den Bree, Joris R. Vermeesch, Therese van Amelsvoort, S. T. Warren, Wendy R. Kates, S. Morrison, Kieran C. Murphy and other authors.

This paper is made freely available by the publisher.

This paper is made freely available by the publisher.

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