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Peer Review reports

From: 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

Original Submission
7 Apr 2016 Submitted Original manuscript
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 2
Submitted Manuscript version 2
Publishing
16 Jun 2016 Editorially accepted
12 Jul 2016 Article published 10.1186/s13053-016-0056-3

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Hereditary Cancer in Clinical Practice

ISSN: 1897-4287