Peer Review reports
From: Whole-exome sequencing enables rapid and prenatal diagnosis of inherited skin disorders
| Original Submission | ||
|---|---|---|
| 21 Aug 2022 | Submitted | Original manuscript |
| Resubmission - Version 2 | ||
| Submitted | Manuscript version 2 | |
| 8 Nov 2022 | Reviewed | Reviewer Report |
| 13 Jun 2023 | Reviewed | Reviewer Report |
| 24 Jun 2023 | Author responded | Author comments - Guo Hong |
| Resubmission - Version 3 | ||
| 24 Jun 2023 | Submitted | Manuscript version 3 |
| 26 Jun 2023 | Author responded | Author comments - Guo Hong |
| Resubmission - Version 4 | ||
| 26 Jun 2023 | Submitted | Manuscript version 4 |
| 4 Jul 2023 | Author responded | Author comments - Guo Hong |
| Resubmission - Version 5 | ||
| 4 Jul 2023 | Submitted | Manuscript version 5 |
| 4 Aug 2023 | Reviewed | Reviewer Report |
| Resubmission - Version 6 | ||
| Submitted | Manuscript version 6 | |
| Publishing | ||
| 7 Aug 2023 | Editorially accepted | |
| 21 Aug 2023 | Article published | 10.1186/s12920-023-01628-2 |
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