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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