Briggs, Tracy A <br/><br/>
Temple syndrome as a result of isolated hypomethylation of the 14q32 imprinted DLK1/MEG3 region.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jan 2016 
 - 170-5 p.  digital 
<br/><br/> Publication Type: Case Reports; 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.37400  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Calcium-Binding Proteins<br/>Chromosomes, Human, Pair 14--genetics<br/>DNA Methylation--genetics<br/>Developmental Disabilities--genetics<br/>Female<br/>Genomic Imprinting--genetics<br/>Humans<br/>Intercellular Signaling Peptides and Proteins--genetics<br/>Membrane Proteins--genetics<br/>Phenotype<br/>RNA, Long Noncoding--genetics<br/>Uniparental Disomy--genetics