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Peer Review reports

From: Concurrent of compound heterozygous variant of a novel in-frame deletion and the common hypomorphic haplotype in TBX6 and inherited 17q12 microdeletion in a fetus

Original Submission
19 Feb 2024 Submitted Original manuscript
14 Apr 2024 Reviewed Reviewer Report
14 Apr 2024 Reviewed Reviewer Report
27 Apr 2024 Author responded Author comments - Shuyuan Li
Resubmission - Version 2
27 Apr 2024 Submitted Manuscript version 2
26 May 2024 Reviewed Reviewer Report
27 May 2024 Reviewed Reviewer Report
31 May 2024 Author responded Author comments - Shuyuan Li
Resubmission - Version 3
31 May 2024 Submitted Manuscript version 3
14 Jun 2024 Reviewed Reviewer Report
17 Jun 2024 Author responded Author comments - Shuyuan Li
Resubmission - Version 4
17 Jun 2024 Submitted Manuscript version 4
Publishing
20 Jun 2024 Editorially accepted
1 Jul 2024 Article published 10.1186/s12884-024-06653-2

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