Fusion-driven Spindle Cell Rhabdomyosarcomas of Bone and Soft Tissue: A Clinicopathologic and Molecular Genetic Study of 25 Cases
Author:
Funder
Mayo Clinic
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference53 articles.
1. WHO Classification of Tumours of Soft Tissue and Bone;Fletcher,2013
2. Soft tissue and bone tumours. WHO Classification of Tumours Series,2020
3. MYOD1 (L122R) mutations are associated with spindle cell and sclerosing rhabdomyosarcomas with aggressive clinical outcomes;Rekhi;Mod Pathol,2016
4. Transactivating mutation of the MYOD1 gene is a frequent event in adult spindle cell rhabdomyosarcoma;Szuhai;J Pathol,2014
5. Recurrent MYOD1 mutations in pediatric and adult sclerosing and spindle cell rhabdomyosarcomas: evidence for a common pathogenesis;Agaram;Genes Chromosomes Cancer,2014
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