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Peer Review reports

From: Three case reports of patients indicating the diversity of molecular and clinical features of 16p11.2 microdeletion anomaly

Original Submission
24 Nov 2020 Submitted Original manuscript
15 Dec 2020 Reviewed Reviewer Report - Rana Fetit
17 Dec 2020 Reviewed Reviewer Report
30 Dec 2020 Reviewed Reviewer Report
26 Jan 2021 Author responded Author comments - Monika Szelest
Resubmission - Version 2
26 Jan 2021 Submitted Manuscript version 2
1 Feb 2021 Reviewed Reviewer Report
6 Feb 2021 Reviewed Reviewer Report
8 Feb 2021 Reviewed Reviewer Report - Rana Fetit
16 Feb 2021 Author responded Author comments - Monika Szelest
Resubmission - Version 3
16 Feb 2021 Submitted Manuscript version 3
24 Feb 2021 Author responded Author comments - Monika Szelest
Resubmission - Version 4
24 Feb 2021 Submitted Manuscript version 4
1 Mar 2021 Author responded Author comments - Monika Szelest
Resubmission - Version 5
1 Mar 2021 Submitted Manuscript version 5
Publishing
3 Mar 2021 Editorially accepted
10 Mar 2021 Article published 10.1186/s12920-021-00929-8

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