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Peer Review reports

From: Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

Original Submission
24 Jul 2021 Submitted Original manuscript
16 Aug 2021 Reviewed Reviewer Report
18 Aug 2021 Reviewed Reviewer Report
8 Sep 2021 Author responded Author comments - Li-Ye Yang
Resubmission - Version 2
8 Sep 2021 Submitted Manuscript version 2
22 Sep 2021 Reviewed Reviewer Report
30 Sep 2021 Author responded Author comments - Li-Ye Yang
Resubmission - Version 3
30 Sep 2021 Submitted Manuscript version 3
7 Oct 2021 Author responded Author comments - Li-Ye Yang
Resubmission - Version 4
7 Oct 2021 Submitted Manuscript version 4
Resubmission - Version 5
Submitted Manuscript version 5
15 Oct 2021 Reviewed Reviewer Report
19 Oct 2021 Reviewed Reviewer Report
2 Nov 2021 Author responded Author comments - Li-Ye Yang
Resubmission - Version 6
2 Nov 2021 Submitted Manuscript version 6
9 Nov 2021 Reviewed Reviewer Report
Resubmission - Version 7
Submitted Manuscript version 7
Publishing
10 Nov 2021 Editorially accepted
11 Dec 2021 Article published 10.1186/s12887-021-03010-6

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