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- W2528367757 abstract "A Polish study has recently revealed an association between CHEK2 I157T polymorphism and an approximately 3-fold elevation of the risk of ovarian border-line carcinoma. The present study was aimed to validate this observation in the genetically similar population, i.e. Russian females. The frequency of the variant CHEK2 allele approached to 9/77 (11,7 %) in patients, but only 35/671 (5,2 %) in controls (р=0,022; OR=2,41 (1,03-5,48), that confirmed the role of genetic predisposition in the etiology of this rare ovarian disease." @default.
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- W2528367757 date "2006-01-01" @default.
- W2528367757 modified "2023-09-26" @default.
- W2528367757 title "Ассоциация между полиморфизмом I157T гена СНЕК2 и риском пограничных серозных опухолей яичника у жительниц России" @default.
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