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pubmed-article:20932739pubmed:abstractTextEpithelioid sarcoma (ES) is a rare soft tissue neoplasm that usually arises in the distal extremities of young adults, presents a high rate of recurrences and metastases and frequently poses diagnostic dilemmas. In order to identify markers useful for patient stratification purposes, we investigated the prognostic impact of clinical and molecular patient characteristics, including the status of SMARCB1 tumour suppressor gene, in a consecutive series of ES cases.lld:pubmed
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pubmed-article:20932739pubmed:copyrightInfoCopyright © 2010 Elsevier Ltd. All rights reserved.lld:pubmed
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pubmed-article:20932739pubmed:articleTitlePrognostic determinants in epithelioid sarcoma.lld:pubmed
pubmed-article:20932739pubmed:affiliationUnit of Molecular Cytogenetics, Fondazione IRCCS Istituto Nazionale Tumori, Milano, Italy.lld:pubmed
pubmed-article:20932739pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20932739pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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