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Publikováno v:
Romanian Journal of Orthopaedic Surgery and Traumatology. 1:58-58
Introduction. Soft Tissue Sarcomas (STS) is a group of rare malignant tumors with mesenchymal tissue origin. At present, over 50 histopathological types with typical chromosome changes are described. Treatment is multidisciplinary, centered on the su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b90455dbd23bccb9c8d4502e68b83345
https://doi.org/10.2478/rojost-2018-0069
https://doi.org/10.2478/rojost-2018-0069
