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Peer Review reports

From: “Liu-Liang-Chung” syndrome with multiple congenital anomalies and the distinctive craniofacial features caused by dominant ZEB2 gene gain mutation

Original Submission
10 Oct 2022 Submitted Original manuscript
14 Nov 2022 Author responded Author comments - weiliang liu
Resubmission - Version 2
14 Nov 2022 Submitted Manuscript version 2
26 Feb 2023 Reviewed Reviewer Report
12 Mar 2023 Reviewed Reviewer Report
30 Jun 2023 Reviewed Reviewer Report
7 Jul 2023 Author responded Author comments - weiliang liu
Resubmission - Version 3
7 Jul 2023 Submitted Manuscript version 3
29 Aug 2023 Reviewed Reviewer Report
30 Aug 2023 Author responded Author comments - weiliang liu
Resubmission - Version 4
30 Aug 2023 Submitted Manuscript version 4
Publishing
14 Sep 2023 Editorially accepted
21 Sep 2023 Article published 10.1186/s12887-023-04314-5

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