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Peer Review reports

From: Novel compound heterozygous mutations of DNAH5 identified in a pediatric patient with Kartagener syndrome: case report and literature review

Original Submission
16 Aug 2020 Submitted Original manuscript
19 Sep 2020 Reviewed Reviewer Report
15 Oct 2020 Reviewed Reviewer Report
17 Dec 2020 Author responded Author comments - Lina Wang
Resubmission - Version 2
17 Dec 2020 Submitted Manuscript version 2
28 Dec 2020 Reviewed Reviewer Report
13 Jan 2021 Reviewed Reviewer Report
7 Feb 2021 Author responded Author comments - Lina Wang
Resubmission - Version 3
7 Feb 2021 Submitted Manuscript version 3
8 Mar 2021 Author responded Author comments - Lina Wang
Resubmission - Version 4
8 Mar 2021 Submitted Manuscript version 4
14 Mar 2021 Author responded Author comments - Lina Wang
Resubmission - Version 5
14 Mar 2021 Submitted Manuscript version 5
17 Mar 2021 Author responded Author comments - Lina Wang
Resubmission - Version 6
17 Mar 2021 Submitted Manuscript version 6
18 Mar 2021 Author responded Author comments - Lina Wang
Resubmission - Version 7
18 Mar 2021 Submitted Manuscript version 7
23 Mar 2021 Author responded Author comments - Lina Wang
Resubmission - Version 8
23 Mar 2021 Submitted Manuscript version 8
21 Jun 2021 Author responded Author comments - Lina Wang
Resubmission - Version 9
21 Jun 2021 Submitted Manuscript version 9
28 Jun 2021 Author responded Author comments - Lina Wang
Resubmission - Version 10
28 Jun 2021 Submitted Manuscript version 10
29 Jun 2021 Author responded Author comments - Lina Wang
Resubmission - Version 11
29 Jun 2021 Submitted Manuscript version 11
Publishing
6 Jul 2021 Editorially accepted
14 Aug 2021 Article published 10.1186/s12890-021-01586-4

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