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De novo variants in FBXO11 cause a syndromic form of intell..:
Jansen, Sandra
;
van der Werf, Ilse M.
;
Innes, A. Micheil
...
European Journal of Human Genetics. 27 (2019) 5 - p. 738-746 , 2019
Link:
https://doi.org/10.1038/s41431-018-0292-2
RT Journal T1
De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_s41431-018-0292-2&Exemplar=1&LAN=DE A1 Jansen, Sandra A1 van der Werf, Ilse M. A1 Innes, A. Micheil A1 Afenjar, Alexandra A1 Agrawal, Pankaj B. A1 Anderson, Ilse J. A1 Atwal, Paldeep S. A1 van Binsbergen, Ellen A1 van den Boogaard, Marie-José A1 Castiglia, Lucia A1 Coban-Akdemir, Zeynep H. A1 van Dijck, Anke A1 Doummar, Diane A1 van Eerde, Albertien M. A1 van Essen, Anthonie J. A1 van Gassen, Koen L. A1 Guillen Sacoto, Maria J. A1 van Haelst, Mieke M. A1 Iossifov, Ivan A1 Jackson, Jessica L. A1 Judd, Elizabeth A1 Kaiwar, Charu A1 Keren, Boris A1 Klee, Eric W. A1 Klein Wassink-Ruiter, Jolien S. A1 Meuwissen, Marije E. A1 Monaghan, Kristin G. A1 de Munnik, Sonja A. A1 Nava, Caroline A1 Ockeloen, Charlotte W. PB Springer Science and Business Media LLC YR 2019 SN 1018-4813 SN 1476-5438 JF European Journal of Human Genetics VO 27 IS 5 SP 738 OP 746 LK http://dx.doi.org/https://doi.org/10.1038/s41431-018-0292-2 DO https://doi.org/10.1038/s41431-018-0292-2 SF ELIB - SuUB Bremen
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