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Peer Review reports

From: Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the literature

Original Submission
16 Dec 2020 Submitted Original manuscript
8 Jan 2021 Author responded Author comments - Lichun Xie
Resubmission - Version 2
8 Jan 2021 Submitted Manuscript version 2
28 Oct 2020 Reviewed Reviewer Report
4 Feb 2021 Author responded Author comments - Lichun Xie
Resubmission - Version 3
4 Feb 2021 Submitted Manuscript version 3
12 Feb 2021 Author responded Author comments - Lichun Xie
Resubmission - Version 4
12 Feb 2021 Submitted Manuscript version 4
Publishing
18 Feb 2021 Editorially accepted
11 Mar 2021 Article published 10.1186/s12920-021-00912-3

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BMC Medical Genomics

ISSN: 1755-8794

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