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Peer Review reports

From: A novel 1p13.2 deletion associates with neurodevelopmental disorders in a three-generation pedigree

Original Submission
3 Jan 2023 Submitted Original manuscript
17 Jan 2023 Reviewed Reviewer Report
25 Jan 2023 Reviewed Reviewer Report
7 Feb 2023 Author responded Author comments - Yan Zhang
Resubmission - Version 2
7 Feb 2023 Submitted Manuscript version 2
15 Feb 2023 Author responded Author comments - Yan Zhang
Resubmission - Version 3
15 Feb 2023 Submitted Manuscript version 3
6 Mar 2023 Author responded Author comments - Yan Zhang
Resubmission - Version 4
6 Mar 2023 Submitted Manuscript version 4
26 Apr 2023 Author responded Author comments - Yan Zhang
Resubmission - Version 5
26 Apr 2023 Submitted Manuscript version 5
2 May 2023 Reviewed Reviewer Report
3 May 2023 Reviewed Reviewer Report
Resubmission - Version 6
Submitted Manuscript version 6
Publishing
5 May 2023 Editorially accepted
23 May 2023 Article published 10.1186/s12920-023-01534-7

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