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Peer Review reports

From: A novel missense mutation of FOXC1 in an Axenfeld–Rieger syndrome patient with a congenital atrial septal defect and sublingual cyst: a case report and literature review

Original Submission
1 Jun 2021 Submitted Original manuscript
5 Aug 2021 Author responded Author comments - Kaiming Li
Resubmission - Version 2
5 Aug 2021 Submitted Manuscript version 2
11 Aug 2021 Author responded Author comments - Kaiming Li
Resubmission - Version 3
11 Aug 2021 Submitted Manuscript version 3
1 Sep 2021 Reviewed Reviewer Report
2 Sep 2021 Reviewed Reviewer Report - Venkateshwari Ananthapur
30 Sep 2021 Author responded Author comments - Kaiming Li
Resubmission - Version 4
30 Sep 2021 Submitted Manuscript version 4
14 Oct 2021 Author responded Author comments - Kaiming Li
Resubmission - Version 5
14 Oct 2021 Submitted Manuscript version 5
15 Oct 2021 Author responded Author comments - Kaiming Li
Resubmission - Version 6
15 Oct 2021 Submitted Manuscript version 6
Publishing
18 Oct 2021 Editorially accepted
29 Oct 2021 Article published 10.1186/s12920-021-01103-w

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