Sparago, Angela <br/><br/>
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.  [electronic resource] 

 -  Nature genetics  Sep 2004 
 - 958-60 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/ng1410  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Beckwith-Wiedemann Syndrome--genetics<br/>CCCTC-Binding Factor<br/>DNA Methylation<br/>DNA-Binding Proteins--genetics<br/>Gene Deletion<br/>Gene Silencing<br/>Genomic Imprinting<br/>Humans<br/>Insulin-Like Growth Factor II--genetics<br/>Molecular Sequence Data<br/>Pedigree<br/>RNA, Long Noncoding<br/>RNA, Untranslated<br/>Repressor Proteins--genetics