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Peer Review reports

From: Clinical and whole-exome sequencing findings in two siblings from Hani ethnic minority with congenital glycosylation disorders

Original Submission
10 Feb 2019 Submitted Original manuscript
27 Mar 2019 Author responded Author comments - Huaiyu Gu
Resubmission - Version 2
27 Mar 2019 Submitted Manuscript version 2
27 May 2019 Author responded Author comments - Huaiyu Gu
Resubmission - Version 3
27 May 2019 Submitted Manuscript version 3
21 Jun 2019 Reviewed Reviewer Report - Kamwing Jair
4 Jul 2019 Reviewed Reviewer Report - Kent Lai
17 Jul 2019 Author responded Author comments - Huaiyu Gu
Resubmission - Version 4
17 Jul 2019 Submitted Manuscript version 4
16 Sep 2019 Reviewed Reviewer Report - Kent Lai
23 Sep 2019 Reviewed Reviewer Report - Kamwing Jair
2 Oct 2019 Author responded Author comments - Huaiyu Gu
Resubmission - Version 5
2 Oct 2019 Submitted Manuscript version 5
Publishing
3 Oct 2019 Editorially accepted
14 Nov 2019 Article published 10.1186/s12881-019-0902-z

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