Astuti, Dewi <br/><br/>
Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility.  [electronic resource] 

 -  Nature genetics  Feb 2012 
 - 277-84 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1546-1718 
<br/><br/><label>Standard No.: </label>10.1038/ng.1071  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Base Sequence<br/>Cell Division--genetics<br/>Cell Proliferation<br/>Child, Preschool<br/>Chromosomes, Human, Pair 2--genetics<br/>Exoribonucleases--genetics<br/>Fetal Macrosomia--genetics<br/>Gene Expression Regulation--genetics<br/>Gene Knockdown Techniques<br/>Genes, cdc--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Germ-Line Mutation--genetics<br/>HeLa Cells<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Kidney Neoplasms--genetics<br/>Molecular Sequence Data<br/>RNA--metabolism<br/>Sequence Analysis, DNA<br/>Wilms Tumor--genetics