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Peer Review reports

From: Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient

Original Submission
17 Aug 2017 Submitted Original manuscript
23 Aug 2017 Author responded Author comments - Zi-Ye ZHAO
Resubmission - Version 2
23 Aug 2017 Submitted Manuscript version 2
18 Sep 2017 Author responded Author comments - Zi-Ye ZHAO
Resubmission - Version 3
18 Sep 2017 Submitted Manuscript version 3
Publishing
27 Sep 2017 Editorially accepted
15 Nov 2017 Article published 10.1186/s12881-017-0471-y

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