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

Authors :: 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
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; 738; 746; 1018-4813; 5; vol. 27; ~European Journal of Human Genetics~738~746~~~1018-4813~5~27~~
Publication Year :: 2019
Abstract: Item does not contain fulltext

Database :: OAIster
Journal :: European Journal of Human Genetics; 738; 746; 1018-4813; 5; vol. 27; ~European Journal of Human Genetics~738~746~~~1018-4813~5~27~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1284083341
Document Type :: Electronic Resource

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