Forest, Fabien <br/><br/>
Conventional chondrosarcoma in a survivor of rhabdoid tumor: enlarging the spectrum of tumors associated with SMARCB1 germline mutations.  [electronic resource] 

 -  The American journal of surgical pathology  Dec 2012 
 - 1892-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1532-0979 
<br/><br/><label>Standard No.: </label>10.1097/PAS.0b013e31826cbe7a  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Biomarkers, Tumor--analysis<br/>Child<br/>Chondrosarcoma--chemistry<br/>Chromosomal Proteins, Non-Histone--analysis<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--analysis<br/>Exons<br/>Gene Deletion<br/>Genetic Predisposition to Disease<br/>Germ-Line Mutation<br/>Humans<br/>Immunohistochemistry<br/>Magnetic Resonance Imaging<br/>Male<br/>Mandibular Neoplasms--chemistry<br/>Neoplasms, Second Primary--chemistry<br/>Rhabdoid Tumor--chemistry<br/>SMARCB1 Protein<br/>Thoracic Neoplasms--chemistry<br/>Tomography, X-Ray Computed<br/>Transcription Factors--analysis