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Peer review reports

From: A novel deletion mutation in the BCOR gene is associated with oculo-facio-cardio-dental syndrome: a case report

Original Submission
17 Jun 2021 Submitted Original manuscript
14 Jul 2021 Reviewed Reviewer Report - Francisco Cammarata-Scalisi
6 Aug 2021 Reviewed Reviewer Report
21 Oct 2021 Author responded Author comments - Qian Hu
Resubmission - Version 2
21 Oct 2021 Submitted Manuscript version 2
20 Nov 2021 Reviewed Reviewer Report
14 Dec 2021 Author responded Author comments - Qian Hu
Resubmission - Version 3
14 Dec 2021 Submitted Manuscript version 3
19 Dec 2021 Reviewed Reviewer Report
20 Dec 2021 Author responded Author comments - Qian Hu
Resubmission - Version 4
20 Dec 2021 Submitted Manuscript version 4
28 Jan 2022 Author responded Author comments - Qian Hu
Resubmission - Version 5
28 Jan 2022 Submitted Manuscript version 5
Publishing
31 Jan 2022 Editorially accepted
7 Feb 2022 Article published 10.1186/s12887-022-03148-x

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