Ockeloen, Charlotte W <br/><br/>
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations.  [electronic resource] 

 -  European journal of human genetics : EJHG  Sep 2015 
 - 1176-85 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2014.253  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adolescent<br/>Adult<br/>Autism Spectrum Disorder--complications<br/>Bone Diseases, Developmental--complications<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 16<br/>DNA Mutational Analysis<br/>Exome<br/>Facies<br/>Female<br/>Gene Deletion<br/>Gene Expression<br/>Genotype<br/>Humans<br/>Intellectual Disability--complications<br/>Male<br/>Middle Aged<br/>Phenotype<br/>Repressor Proteins--genetics<br/>Tooth Abnormalities--complications