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Peer Review reports

From: Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome family

Original Submission
14 May 2023 Submitted Original manuscript
12 Jun 2023 Reviewed Reviewer Report - Navneesh Yadav
15 Aug 2023 Reviewed Reviewer Report - Sabyasachi Senapati
11 Sep 2023 Author responded Author comments - Shi-Hao Chen
Resubmission - Version 2
11 Sep 2023 Submitted Manuscript version 2
12 Sep 2023 Author responded Author comments - Shi-Hao Chen
Resubmission - Version 3
12 Sep 2023 Submitted Manuscript version 3
12 Sep 2023 Author responded Author comments - Shi-Hao Chen
Resubmission - Version 4
12 Sep 2023 Submitted Manuscript version 4
1 Oct 2023 Reviewed Reviewer Report - Navneesh Yadav
15 Oct 2023 Reviewed Reviewer Report
24 Oct 2023 Author responded Author comments - Shi-Hao Chen
Resubmission - Version 5
24 Oct 2023 Submitted Manuscript version 5
24 Oct 2023 Reviewed Reviewer Report
Resubmission - Version 6
Submitted Manuscript version 6
Publishing
27 Oct 2023 Editorially accepted
7 Nov 2023 Article published 10.1186/s12886-023-03189-5

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