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Peer Review reports

From: A novel heterozygous mutation of CHD7 gene in a Chinese patient with Kallmann syndrome: a case report

Original Submission
22 Oct 2020 Submitted Original manuscript
20 Nov 2020 Author responded Author comments - Weiwei Xu
Resubmission - Version 2
20 Nov 2020 Submitted Manuscript version 2
6 Dec 2020 Author responded Author comments - Weiwei Xu
Resubmission - Version 3
6 Dec 2020 Submitted Manuscript version 3
18 Jan 2021 Author responded Author comments - Weiwei Xu
Resubmission - Version 4
18 Jan 2021 Submitted Manuscript version 4
1 Mar 2021 Reviewed Reviewer Report - Maria Cristina Azcona-Sanjulian
15 Mar 2021 Reviewed Reviewer Report
13 Apr 2021 Author responded Author comments - Weiwei Xu
Resubmission - Version 5
13 Apr 2021 Submitted Manuscript version 5
25 May 2021 Reviewed Reviewer Report - Maria Cristina Azcona-Sanjulian
13 Jun 2021 Reviewed Reviewer Report
9 Jul 2021 Author responded Author comments - Weiwei Xu
Resubmission - Version 6
9 Jul 2021 Submitted Manuscript version 6
3 Aug 2021 Author responded Author comments - Weiwei Xu
Resubmission - Version 7
3 Aug 2021 Submitted Manuscript version 7
Publishing
5 Aug 2021 Editorially accepted
25 Sep 2021 Article published 10.1186/s12902-021-00836-0

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