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Peer Review reports

From: Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family

Original Submission
29 Oct 2021 Submitted Original manuscript
23 Nov 2021 Author responded Author comments - Jing Chen
Resubmission - Version 2
23 Nov 2021 Submitted Manuscript version 2
6 Feb 2022 Reviewed Reviewer Report
11 Apr 2022 Reviewed Reviewer Report
11 May 2022 Author responded Author comments - Jing Chen
Resubmission - Version 3
11 May 2022 Submitted Manuscript version 3
19 Jun 2022 Author responded Author comments - Jing Chen
Resubmission - Version 4
19 Jun 2022 Submitted Manuscript version 4
Publishing
22 Jun 2022 Editorially accepted
8 Jul 2022 Article published 10.1186/s12920-022-01296-8

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