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A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome

Crossref DOI link: https://doi.org/10.1186/s13053-016-0056-3

Published Online: 2016-07-12

Published Print: 2016-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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