Visser, Remco <br/><br/>
RNF135 mutations are not present in patients with Sotos syndrome-like features.  [electronic resource] 

 -  American journal of medical genetics. Part A  Feb 2009 
 - 806-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.32694  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Carrier Proteins--genetics<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Craniofacial Abnormalities--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Genes, Neurofibromatosis 1<br/>Growth Disorders--genetics<br/>Histone Methyltransferases<br/>Histone-Lysine N-Methyltransferase<br/>Humans<br/>Infant<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>Learning Disabilities--genetics<br/>Male<br/>Middle Aged<br/>Mutation<br/>Nuclear Proteins--genetics<br/>Phenotype<br/>Syndrome<br/>Ubiquitin-Protein Ligases<br/>Young Adult