Peer Review reports
From: Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
| Original Submission | ||
|---|---|---|
| 1 May 2020 | Submitted | Original manuscript |
| 10 Jun 2020 | Author responded | Author comments - Tania Espinosa Reyes |
| Resubmission - Version 2 | ||
| 10 Jun 2020 | Submitted | Manuscript version 2 |
| 18 Jun 2020 | Author responded | Author comments - Tania Espinosa Reyes |
| Resubmission - Version 3 | ||
| 18 Jun 2020 | Submitted | Manuscript version 3 |
| 5 Jul 2020 | Reviewed | Reviewer Report |
| 27 Aug 2020 | Reviewed | Reviewer Report |
| 28 Sep 2020 | Author responded | Author comments - Tania Espinosa Reyes |
| Resubmission - Version 4 | ||
| 28 Sep 2020 | Submitted | Manuscript version 4 |
| Publishing | ||
| 22 Oct 2020 | Editorially accepted | |
| 9 Nov 2020 | Article published | 10.1186/s12902-020-00643-z |
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