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Peer Review reports

From: Genetic investigation of 211 Chinese families expands the mutational and phenotypical spectra of hereditary retinopathy genes through targeted sequencing technology

Original Submission
3 Apr 2020 Submitted Original manuscript
11 May 2020 Reviewed Reviewer Report
21 Oct 2020 Reviewed Reviewer Report
19 Nov 2020 Author responded Author comments - Zhouxian Bai
Resubmission - Version 2
19 Nov 2020 Submitted Manuscript version 2
15 Dec 2020 Author responded Author comments - Zhouxian Bai
Resubmission - Version 3
15 Dec 2020 Submitted Manuscript version 3
22 Jan 2021 Author responded Author comments - Zhouxian Bai
Resubmission - Version 4
22 Jan 2021 Submitted Manuscript version 4
15 Feb 2021 Author responded Author comments - Zhouxian Bai
Resubmission - Version 5
15 Feb 2021 Submitted Manuscript version 5
18 Feb 2021 Author responded Author comments - Zhouxian Bai
Resubmission - Version 6
18 Feb 2021 Submitted Manuscript version 6
2 Mar 2021 Author responded Author comments - Zhouxian Bai
Resubmission - Version 7
2 Mar 2021 Submitted Manuscript version 7
4 Mar 2021 Author responded Author comments - Zhouxian Bai
Resubmission - Version 8
4 Mar 2021 Submitted Manuscript version 8
Publishing
8 Mar 2021 Editorially accepted
29 Mar 2021 Article published 10.1186/s12920-021-00935-w

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