Parast, Mana M <br/><br/>
A unique case of renal carcinoma with Xp11.2 translocations/ TFE3 gene fusions in a 3-year-old child, with coexistent von Hippel-Lindau gene mutation.  [electronic resource] 

 -  Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society   
 - 403-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1093-5266 
<br/><br/><label>Standard No.: </label>10.1007/s10024-004-1018-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Artificial Gene Fusion<br/>Basic Helix-Loop-Helix Leucine Zipper Transcription Factors<br/>Carcinoma, Renal Cell--genetics<br/>Child, Preschool<br/>DNA-Binding Proteins--genetics<br/>Diagnosis, Differential<br/>Humans<br/>Kidney Neoplasms--genetics<br/>Mutation<br/>Transcription Factors--genetics<br/>Translocation, Genetic<br/>Tumor Suppressor Proteins--genetics<br/>Ubiquitin-Protein Ligases--genetics<br/>Von Hippel-Lindau Tumor Suppressor Protein