Zarate, Yuri A <br/><br/>
Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing.  [electronic resource] 

 -  American journal of medical genetics. Part A  May 2015 
 - 1026-32 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.36849  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 2--genetics<br/>Cleft Palate--genetics<br/>Codon, Nonsense--genetics<br/>Craniofacial Abnormalities--genetics<br/>Exome--genetics<br/>Female<br/>Frameshift Mutation--genetics<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Intellectual Disability--genetics<br/>Language Development Disorders--genetics<br/>Male<br/>Matrix Attachment Region Binding Proteins--genetics<br/>Transcription Factors--genetics