Strong evidence that the common variant S384F inBRCA2has no...

Strong evidence that the common variant S384F inBRCA2has no pathogenic relevance in hereditary breast cancer

B Wappenschmidt, R Fimmers, K Rhiem, M Brosig, E Wardelmann…
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Volume:
7
Language:
english
DOI:
10.1186/bcr1291
Date:
October, 2005
File:
PDF, 664 KB
english, 2005
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