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Peer Review reports

From: Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome

Original Submission
20 Mar 2018 Submitted Original manuscript
22 Jul 2018 Reviewed Reviewer Report - Shiwani Sharma
3 Aug 2018 Reviewed Reviewer Report - John Rosendahl Østergaard
26 Aug 2018 Author responded Author comments - CHAO LING
Resubmission - Version 2
26 Aug 2018 Submitted Manuscript version 2
7 Sep 2018 Reviewed Reviewer Report - John Rosendahl Østergaard
18 Sep 2018 Reviewed Reviewer Report - Shiwani Sharma
11 Oct 2018 Author responded Author comments - CHAO LING
Resubmission - Version 3
11 Oct 2018 Submitted Manuscript version 3
5 Nov 2018 Author responded Author comments - CHAO LING
Resubmission - Version 4
5 Nov 2018 Submitted Manuscript version 4
15 Nov 2018 Author responded Author comments - CHAO LING
Resubmission - Version 5
15 Nov 2018 Submitted Manuscript version 5
Publishing
21 Nov 2018 Editorially accepted
14 Jan 2019 Article published 10.1186/s12881-018-0725-3

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