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Peer Review reports

From: Intronic mutation of the VHL gene associated with central nervous system hemangioblastomas in two Chinese families with Von Hippel–Lindau disease: case report

Original Submission
6 May 2020 Submitted Original manuscript
16 May 2020 Author responded Author comments - Zhen Liu
Resubmission - Version 2
16 May 2020 Submitted Manuscript version 2
20 Jun 2020 Reviewed Reviewer Report
29 Jun 2020 Reviewed Reviewer Report - Bianca Bianco
13 Jul 2020 Author responded Author comments - Zhen Liu
Resubmission - Version 3
13 Jul 2020 Submitted Manuscript version 3
2 Aug 2020 Reviewed Reviewer Report
19 Aug 2020 Reviewed Reviewer Report
8 Sep 2020 Author responded Author comments - Zhen Liu
Resubmission - Version 4
8 Sep 2020 Submitted Manuscript version 4
9 Sep 2020 Author responded Author comments - Zhen Liu
Resubmission - Version 5
9 Sep 2020 Submitted Manuscript version 5
11 Sep 2020 Author responded Author comments - Zhen Liu
Resubmission - Version 6
11 Sep 2020 Submitted Manuscript version 6
14 Sep 2020 Author responded Author comments - Zhen Liu
Resubmission - Version 7
14 Sep 2020 Submitted Manuscript version 7
Publishing
21 Sep 2020 Editorially accepted
1 Oct 2020 Article published 10.1186/s12881-020-01126-7

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