De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms

Find Full text
Publication year
2019
Author(s)
Jansen, S
Werf, I. van der
Innes, A. Micheil
Afenjar, A.
Agrawal, Pankaj B.
Anderson, I.J.
Munnik, Sonja A. de
Ockeloen, C.W.
Rinne, T.K.
Vries, P.F. de
Pfundt, R.P.
Veltman, J.A.
Vissers, L.E.L.M.
Vries, B.B.A. de
Source
European Journal of Human Genetics, 27, 5, (2019), pp. 738-746
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/202998   https://hdl.handle.net/2066/202998
Display more details

Upload full text

Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.