De Novo Variants in FBXO11 Cause a Syndromic Form of Intellectual Disability with Behavioral Problems and Dysmorphisms

Sandra Jansen,Ilse M. van der Werf,A. Micheil Innes,Alexandra Afenjar,Pankaj B. Agrawal,Ilse J. Anderson,Paldeep S. Atwal,Ellen van Binsbergen,Marie-José van den Boogaard,Lucia Castiglia,Zeynep H. Coban-Akdemir,Anke van Dijck,Diane Doummar,Albertien M. van Eerde,Anthonie J. van Essen,Koen L. van Gassen,Maria J. Guillen Sacoto,Mieke M. van Haelst,Ivan Iossifov,Jessica L. Jackson, Elizabeth Judd,Charu Kaiwar,Boris Keren,Eric W. Klee,Jolien S. Klein Wassink-Ruiter,Marije E. Meuwissen,Kristin G. Monaghan,Sonja A. de Munnik,Caroline Nava,Charlotte W. Ockeloen,Rosa Pettinato,Hilary Racher,Tuula Rinne,Corrado Romano,Victoria R. Sanders,Rhonda E. Schnur,Eric J. Smeets,Alexander P. A. Stegmann,Asbjørg Stray-Pedersen,David A. Sweetser,Paulien A. Terhal,Kristian Tveten,Grace E. VanNoy,Petra F. de Vries,Jessica L. Waxler,Marcia Willing,Rolph Pfundt,Joris A. Veltman,R. Frank Kooy,Lisenka E. L. M. Vissers,Bert B. A. de Vries

European journal of human genetics（2019）

引用 28|浏览61

暂无评分

关键词

Disease genetics,Genetics of the nervous system,Neurodevelopmental disorders,Biomedicine,general,Human Genetics,Bioinformatics,Gene Expression,Cytogenetics

AI 理解论文

溯源树

样例

生成溯源树，研究论文发展脉络

Chat Paper

正在生成论文摘要