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Peer Review reports

From: An ultra-rare case of immunoskeletal dysplasia with neurodevelopmental abnormalities in an Indian patient with homozygous c.953C > T variant in EXTL3 gene: a case report

Original Submission
29 Aug 2021 Submitted Original manuscript
29 Sep 2021 Reviewed Reviewer Report
9 Oct 2021 Reviewed Reviewer Report
9 Oct 2021 Reviewed Reviewer Report
12 Oct 2021 Reviewed Reviewer Report
15 Nov 2021 Author responded Author comments - Shruti Bajaj
Resubmission - Version 2
15 Nov 2021 Submitted Manuscript version 2
28 Nov 2021 Reviewed Reviewer Report
8 Dec 2021 Reviewed Reviewer Report
23 Dec 2021 Author responded Author comments - Shruti Bajaj
Resubmission - Version 3
23 Dec 2021 Submitted Manuscript version 3
Publishing
26 Jan 2022 Editorially accepted
3 Feb 2022 Article published 10.1186/s12887-022-03143-2

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