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FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor. [electronic resource] by
Producer: 20160531 In: Human molecular genetics vol. 24
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Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction. [electronic resource] by
Producer: 20110210 In: Cancer research vol. 70
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