Beygo, Jasmin <br/><br/>
New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome.  [electronic resource] 

 -  European journal of human genetics : EJHG  08 2017 
 - 935-945 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.2017.91  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Chromosome Disorders--diagnosis<br/>Chromosomes, Human, Pair 14--genetics<br/>DNA Methylation<br/>Female<br/>Genomic Imprinting<br/>Humans<br/>Infant<br/>Male<br/>Middle Aged<br/>RNA, Long Noncoding--genetics<br/>RNA, Small Nucleolar--genetics