De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms
SourceEuropean Journal of Human Genetics, 27, 5, (2019), pp. 738-746
Article / Letter to editor
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European Journal of Human Genetics
SubjectAll institutes and research themes of the Radboud University Medical Center; Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience; Radboudumc 9: Rare cancers RIHS: Radboud Institute for Health Sciences
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