Baple, Emma L <br/><br/>
An atypical case of hypomethylation at multiple imprinted loci.  [electronic resource] 

 -  European journal of human genetics : EJHG  Mar 2011 
 - 360-2 p.  digital 
<br/><br/> Publication Type: Case Reports; 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.2010.218  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Angelman Syndrome--genetics<br/>Beckwith-Wiedemann Syndrome--genetics<br/>Child, Preschool<br/>DNA Methylation<br/>Epigenomics<br/>Female<br/>Genetic Loci<br/>Genomic Imprinting<br/>Humans<br/>Multigene Family<br/>Mutation<br/>Prader-Willi Syndrome--genetics