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Peer Review reports

From: Prenatal diagnosis to identify compound heterozygous variants in PKDCC that causes rhizomelic limb shortening with dysmorphic features in a fetus from China

Original Submission
21 Apr 2023 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
Resubmission - Version 3
Submitted Manuscript version 3
7 Jul 2023 Reviewed Reviewer Report
15 Jul 2023 Reviewed Reviewer Report
17 Jul 2023 Reviewed Reviewer Report - Stetson Thacker
20 Jul 2023 Reviewed Reviewer Report - Nicola Marziliano
1 Aug 2023 Author responded Author comments - Haibo Li
Resubmission - Version 4
1 Aug 2023 Submitted Manuscript version 4
6 Aug 2023 Reviewed Reviewer Report
8 Aug 2023 Reviewed Reviewer Report - Stetson Thacker
10 Aug 2023 Reviewed Reviewer Report - Nicola Marziliano
Resubmission - Version 5
Submitted Manuscript version 5
Publishing
11 Aug 2023 Editorially accepted
17 Aug 2023 Article published 10.1186/s12920-023-01631-7

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