Peer Review reports
From: Atypical deletion of Williams–Beuren syndrome reveals the mechanism of neurodevelopmental disorders
| Original Submission | ||
|---|---|---|
| 24 Nov 2021 | Submitted | Original manuscript |
| 13 Dec 2021 | Reviewed | Reviewer Report |
| 21 Dec 2021 | Reviewed | Reviewer Report |
| 16 Jan 2022 | Author responded | Author comments - Jimei Chen |
| Resubmission - Version 2 | ||
| 16 Jan 2022 | Submitted | Manuscript version 2 |
| 28 Jan 2022 | Author responded | Author comments - Jimei Chen |
| Resubmission - Version 3 | ||
| 28 Jan 2022 | Submitted | Manuscript version 3 |
| 24 Feb 2022 | Author responded | Author comments - Jimei Chen |
| Resubmission - Version 4 | ||
| 24 Feb 2022 | Submitted | Manuscript version 4 |
| 15 Mar 2022 | Reviewed | Reviewer Report |
| 16 Mar 2022 | Reviewed | Reviewer Report |
| 18 Mar 2022 | Author responded | Author comments - Jimei Chen |
| Resubmission - Version 5 | ||
| 18 Mar 2022 | Submitted | Manuscript version 5 |
| 25 Mar 2022 | Reviewed | Reviewer Report |
| Resubmission - Version 6 | ||
| Submitted | Manuscript version 6 | |
| Publishing | ||
| 29 Mar 2022 | Editorially accepted | |
| 4 Apr 2022 | Article published | 10.1186/s12920-022-01227-7 |
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