Nonrhabdomyosarcoma soft tissue sarcomas (NRSTS) are relatively rare tumors, which nonetheless constitute 50% of the soft tissue sarcomas seen in the pediatric population. The prognosis for these tumors is good, with 92% of patients in our series alive and 61 % free of their disease at 5 years follo
β¦ LIBER β¦
Pediatric Bone and Soft Tissue Sarcomas
β Scribed by Dr John A Heath
- Book ID
- 108955129
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 28 KB
- Volume
- 42
- Category
- Article
- ISSN
- 1034-4810
No coin nor oath required. For personal study only.
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