Parry, David A <br/><br/>
Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.  [electronic resource] 

 -  American journal of human genetics  Sep 2011 
 - 451-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2011.08.002  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing--genetics<br/>Base Sequence<br/>Cell Line<br/>Female<br/>Genes, Recessive--genetics<br/>Genomic Imprinting--genetics<br/>Humans<br/>Hydatidiform Mole--genetics<br/>Immunohistochemistry<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Oocytes--metabolism<br/>Pedigree<br/>Pregnancy<br/>Proteins--genetics<br/>Sequence Alignment<br/>Sequence Analysis, DNA