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Peer Review reports

From: The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapy

Original Submission
24 Dec 2019 Submitted Original manuscript
16 Jan 2020 Author responded Author comments - Xuyun Hu
Resubmission - Version 2
16 Jan 2020 Submitted Manuscript version 2
25 Feb 2020 Reviewed Reviewer Report
28 Apr 2020 Reviewed Reviewer Report
21 May 2020 Author responded Author comments - Xuyun Hu
Resubmission - Version 3
21 May 2020 Submitted Manuscript version 3
4 Oct 2020 Reviewed Reviewer Report
7 Oct 2020 Reviewed Reviewer Report
20 Oct 2020 Author responded Author comments - Xuyun Hu
Resubmission - Version 4
20 Oct 2020 Submitted Manuscript version 4
20 Nov 2020 Author responded Author comments - Xuyun Hu
Resubmission - Version 5
20 Nov 2020 Submitted Manuscript version 5
Publishing
23 Nov 2020 Editorially accepted
4 Dec 2020 Article published 10.1186/s12920-020-00831-9

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BMC Medical Genomics

ISSN: 1755-8794

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