Jansen, Sandra <br/><br/>
De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms.  [electronic resource] 

 -  European journal of human genetics : EJHG  05 2019 
 - 738-746 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/s41431-018-0292-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Behavior<br/>F-Box Proteins--genetics<br/>Gene Deletion<br/>Genetic Variation<br/>Humans<br/>Intellectual Disability--genetics<br/>Protein-Arginine N-Methyltransferases--genetics<br/>Syndrome