A recurrent chondromyxoid fibroma with chromosome aberrations ins(5;2)(q13;p21p25) and 2p deletion: a case report.
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S. Knuutila | A. Kaipainen | T. Böhling | H. Heliö | E. Karaharju | M. Tarkkanen | J. Szymańska | I. Elomaa
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