RecurrentMYOD1mutations in pediatric and adult sclerosing and spindle cell rhabdomyosarcomas: Evidence for a common pathogenesis
Author:
Affiliation:
1. Department of Pathology; Memorial Sloan Kettering Cancer Center; New York NY
2. Department of Pediatric Surgery; Memorial Sloan Kettering Cancer Center; New York NY
3. Department of Pediatrics; Memorial Sloan Kettering Cancer Center; New York NY
Funder
NIH
Publisher
Wiley
Subject
Cancer Research,Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/gcc.22187/fullpdf
Reference22 articles.
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3. SNP genotyping of a sclerosing rhabdomyosarcoma: Reveals highly aneuploid profile and a specific MDM2/HMGA2 amplification;Bouron-Dal Soglio;Hum Pathol,2009
4. Spindle cell rhabdomyosarcoma. A prognostically favorable variant of rhabdomyosarcoma;Cavazzana;Am J Surg Pathol,1992
5. Sclerosing rhabdomyosarcomas in children and adolescents: A clinicopathologic review of 13 cases from the Intergroup Rhabdomyosarcoma Study Group and Children's Oncology Group;Chiles;Pediatr Dev Pathol,2004
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