Armstrong, Amy E <br/><br/>
A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children's Oncology Group study.  [electronic resource] 

 -  PloS one  2018 
 - e0208936 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0208936  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anaplasia--genetics<br/>Carcinogenesis--genetics<br/>DNA Methylation--genetics<br/>Female<br/>Germ-Line Mutation--genetics<br/>HEK293 Cells<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Kidney--growth & development<br/>Kidney Neoplasms--genetics<br/>Loss of Function Mutation--genetics<br/>Male<br/>Risk Factors<br/>Tripartite Motif-Containing Protein 28--genetics<br/>Wilms Tumor--genetics