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Peer Review reports

From: A novel phenotype of 13q12.3 microdeletion characterized by epilepsy in an Asian child: a case report

Original Submission
9 Jul 2020 Submitted Original manuscript
7 Aug 2020 Reviewed Reviewer Report
15 Aug 2020 Reviewed Reviewer Report - Kohei Aoyama
3 Sep 2020 Author responded Author comments - Mina Wang
Resubmission - Version 2
3 Sep 2020 Submitted Manuscript version 2
5 Sep 2020 Author responded Author comments - Mina Wang
Resubmission - Version 3
5 Sep 2020 Submitted Manuscript version 3
9 Sep 2020 Author responded Author comments - Mina Wang
Resubmission - Version 4
9 Sep 2020 Submitted Manuscript version 4
12 Sep 2020 Author responded Author comments - Mina Wang
Resubmission - Version 5
12 Sep 2020 Submitted Manuscript version 5
17 Sep 2020 Author responded Author comments - Mina Wang
Resubmission - Version 6
17 Sep 2020 Submitted Manuscript version 6
Publishing
22 Sep 2020 Editorially accepted
6 Oct 2020 Article published 10.1186/s12920-020-00801-1

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