Genomic complexity in pediatric synovial sarcomas (Synobio study): the European pediatric soft tissue sarcoma group (EpSSG) experience
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Title
Genomic complexity in pediatric synovial sarcomas (Synobio study): the European pediatric soft tissue sarcoma group (EpSSG) experience
Authors
Keywords
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Journal
Cancer Medicine
Volume 7, Issue 4, Pages 1384-1393
Publisher
Wiley
Online
2018-03-15
DOI
10.1002/cam4.1415
References
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Related references
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- Histotype-tailored neoadjuvant chemotherapy versus standard chemotherapy in patients with high-risk soft-tissue sarcomas (ISG-STS 1001): an international, open-label, randomised, controlled, phase 3, multicentre trial
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- Soft tissue sarcomas in adolescents and young adults: a comparison with their paediatric and adult counterparts
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- RNA sequencing validation of the Complexity INdex in SARComas prognostic signature
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- Recent insights into the biology of neuroblastoma
- (2014) Gudrun Schleiermacher et al. INTERNATIONAL JOURNAL OF CANCER
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- Comparing children and adults with synovial sarcoma in the Surveillance, Epidemiology, and End Results program, 1983 to 2005
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- (2009) Yan Sun et al. CANCER SCIENCE
- Neo/adjuvant chemotherapy does not improve outcome in resected primary synovial sarcoma: a study of the French Sarcoma Group
- (2008) A. Italiano et al. ANNALS OF ONCOLOGY
- Synovial sarcoma of children and adolescents: The prognostic role of axial sites
- (2008) Andrea Ferrari et al. EUROPEAN JOURNAL OF CANCER
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