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Peer Review reports

From: A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case report

Original Submission
16 Dec 2020 Submitted Original manuscript
11 Jan 2021 Author responded Author comments - Panicos Shangaris
Resubmission - Version 2
11 Jan 2021 Submitted Manuscript version 2
16 Jan 2021 Author responded Author comments - Panicos Shangaris
Resubmission - Version 3
16 Jan 2021 Submitted Manuscript version 3
30 Jan 2021 Author responded Author comments - Panicos Shangaris
Resubmission - Version 4
30 Jan 2021 Submitted Manuscript version 4
2 Feb 2021 Author responded Author comments - Panicos Shangaris
Resubmission - Version 5
2 Feb 2021 Submitted Manuscript version 5
5 Feb 2021 Author responded Author comments - Panicos Shangaris
Resubmission - Version 6
5 Feb 2021 Submitted Manuscript version 6
9 Feb 2021 Author responded Author comments - Panicos Shangaris
Resubmission - Version 7
9 Feb 2021 Submitted Manuscript version 7
Publishing
11 Feb 2021 Editorially accepted
26 Feb 2021 Article published 10.1186/s12920-021-00901-6

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