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We selected 5 oncogenes with well-established roles in carcinogenesis -- CCND1, ErbB1, ErbB2, c-myc and ZNF217 -- to investigate the coexistence of their copy imbalances in relation to the clinico-pathological characteristics of ovarian tumors.

Coexistence of Copy Number Increases of <i>c-Myc, ZNF217, CCND1, ErbB1</i> and <i>ErbB2</i> in Ovarian Cancers