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Peer Review reports

From: A novel missense mutation in the MECOM gene in a Chinese boy with radioulnar synostosis with amegakaryocytic thrombocytopenia

Original Submission
4 Sep 2023 Submitted Original manuscript
23 Oct 2023 Reviewed Reviewer Report - Engy Asem
28 Oct 2023 Reviewed Reviewer Report - Canan Albayrak
8 Nov 2023 Reviewed Reviewer Report
13 Dec 2023 Author responded Author comments - Xiaoxi Lu
Resubmission - Version 2
13 Dec 2023 Submitted Manuscript version 2
20 Dec 2023 Author responded Author comments - Xiaoxi Lu
Resubmission - Version 3
20 Dec 2023 Submitted Manuscript version 3
21 Dec 2023 Author responded Author comments - Xiaoxi Lu
Resubmission - Version 4
21 Dec 2023 Submitted Manuscript version 4
27 Dec 2023 Reviewed Reviewer Report - Engy Asem
8 Jan 2024 Reviewed Reviewer Report
10 Jan 2024 Reviewed Reviewer Report - Canan Albayrak
Resubmission - Version 5
Submitted Manuscript version 5
Publishing
11 Jan 2024 Editorially accepted
20 Jan 2024 Article published 10.1186/s12887-024-04552-1

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