ADULT SOFT TISSUE SARCOMA
Identifieur interne : 00AF52 ( Main/Exploration ); précédent : 00AF51; suivant : 00AF53ADULT SOFT TISSUE SARCOMA
Auteurs : G. Bruce Mann ; Jonathan J. Lewis [États-Unis] ; Murray F. Brennan [États-Unis]Source :
- Australian and New Zealand Journal of Surgery [ 0004-8682 ] ; 1999-05.
Abstract
Background: Soft tissue sarcomas (STS) are a group of anatomically and histologically diverse tumours. They account for about 1% of adult malignancies, and about 50% of patients diagnosed with sarcoma eventually die of the disease. These tumours are grouped together because of shared biological characteristics and treatment responses.
Url:
DOI: 10.1046/j.1440-1622.1999.01568.x
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 002608
- to stream Istex, to step Curation: 002608
- to stream Istex, to step Checkpoint: 003873
- to stream Main, to step Merge: 00B570
- to stream Main, to step Curation: 00AF52
Le document en format XML
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<front><div type="abstract">Background: Soft tissue sarcomas (STS) are a group of anatomically and histologically diverse tumours. They account for about 1% of adult malignancies, and about 50% of patients diagnosed with sarcoma eventually die of the disease. These tumours are grouped together because of shared biological characteristics and treatment responses.</div>
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