Peer Review reports
From: Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease
| Original Submission | ||
|---|---|---|
| 19 Feb 2018 | Submitted | Original manuscript |
| 23 Feb 2018 | Author responded | Author comments - Ehsan Razmara |
| Resubmission - Version 2 | ||
| 23 Feb 2018 | Submitted | Manuscript version 2 |
| 8 May 2018 | Reviewed | Reviewer Report - GillianM. Blue |
| 17 May 2018 | Reviewed | Reviewer Report - Nejat Mahdieh |
| 27 May 2018 | Author responded | Author comments - Ehsan Razmara |
| Resubmission - Version 3 | ||
| 27 May 2018 | Submitted | Manuscript version 3 |
| 31 May 2018 | Reviewed | Reviewer Report - Nejat Mahdieh |
| 4 Jun 2018 | Reviewed | Reviewer Report - GillianM. Blue |
| 19 Jun 2018 | Author responded | Author comments - Ehsan Razmara |
| Resubmission - Version 4 | ||
| 19 Jun 2018 | Submitted | Manuscript version 4 |
| Publishing | ||
| 20 Jun 2018 | Editorially accepted | |
| 3 Jul 2018 | Article published | 10.1186/s12872-018-0867-4 |
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