Skip to main content

Peer Review reports

From: Clinical application of non-invasive prenatal diagnosis of phenylketonuria based on haplotypes via paired-end molecular tags and weighting algorithm

Original Submission
12 Jul 2021 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
24 Aug 2021 Reviewed Reviewer Report
25 Aug 2021 Reviewed Reviewer Report - W. Allen Hogge
7 Sep 2021 Author responded Author comments - Kong Xiangdong
Resubmission - Version 3
7 Sep 2021 Submitted Manuscript version 3
13 Sep 2021 Author responded Author comments - Kong Xiangdong
Resubmission - Version 4
13 Sep 2021 Submitted Manuscript version 4
20 Sep 2021 Author responded Author comments - Kong Xiangdong
Resubmission - Version 5
20 Sep 2021 Submitted Manuscript version 5
21 Sep 2021 Author responded Author comments - Kong Xiangdong
Resubmission - Version 6
21 Sep 2021 Submitted Manuscript version 6
4 Oct 2021 Reviewed Reviewer Report - W. Allen Hogge
15 Oct 2021 Reviewed Reviewer Report
3 Nov 2021 Author responded Author comments - Kong Xiangdong
Resubmission - Version 7
3 Nov 2021 Submitted Manuscript version 7
Publishing
1 Dec 2021 Editorially accepted
17 Dec 2021 Article published 10.1186/s12920-021-01141-4

You can find further information about peer review here.

Back to article page