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From: Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families

Original Submission
10 Dec 2019 Submitted Original manuscript
23 Jan 2020 Reviewed Reviewer Report
19 Feb 2020 Reviewed Reviewer Report
2 Apr 2020 Author responded Author comments - Yingjie Zhou
Resubmission - Version 2
2 Apr 2020 Submitted Manuscript version 2
3 Apr 2020 Reviewed Reviewer Report
8 Apr 2020 Reviewed Reviewer Report
19 Jun 2020 Author responded Author comments - Yingjie Zhou
Resubmission - Version 3
19 Jun 2020 Submitted Manuscript version 3
26 Jun 2020 Author responded Author comments - Yingjie Zhou
Resubmission - Version 4
26 Jun 2020 Submitted Manuscript version 4
3 Jul 2020 Author responded Author comments - Yingjie Zhou
Resubmission - Version 5
3 Jul 2020 Submitted Manuscript version 5
Publishing
6 Jul 2020 Editorially accepted
18 Jul 2020 Article published 10.1186/s12881-020-01087-x

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