De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype [Correction]

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Publication year
2017
Author(s)
Shashi, V.
Pena, L.D.
Kim, K.
Burton, B.
Hempel, M.
Schoch, K.
Walkiewicz, M.
McLaughlin, H.M.
Cho, M
Stong, N.
Hickey, S.E.
Shuss, C.M.
Freemark, M.S.
Bellet, J.S.
Keels, M.A.
Bonner, M.J.
El-Dairi, M.
Butler, M
Kranz, P.G.
Stumpel, C.T.
Klinkenberg, S.
Oberndorff, K.
Alawi, M.
Santer, R.
Petrovski, S.
Kuismin, O.
Korpi-Heikkila, S.
Pietilainen, O.
Aarno, P.
Kurki, M.I.
Hoischen, A.
Need, A.C.
Goldstein, D.B
Kortum, F.
Number of pages
1 p.
Source
American Journal of Human Genetics, 100, 1, (2017), pp. 179
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/170308   https://hdl.handle.net/2066/170308
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