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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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