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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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PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS. [electronic resource] by
Producer: 20170825 In: Journal of medical genetics vol. 53
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