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Peer Review reports

From: A case report and mechanism analysis of a normal phenotype mosaic 47, XXY complicated by paternal iUPD (9) who had a normal PGD result

Original Submission
7 Mar 2019 Submitted Original manuscript
19 Apr 2019 Reviewed Reviewer Report - Daniela Zuccarello
20 May 2019 Reviewed Reviewer Report - Tarani Luigi
5 Jun 2019 Reviewed Reviewer Report - Faustina Lalatta
30 Jun 2019 Author responded Author comments - Dan Li
Resubmission - Version 2
30 Jun 2019 Submitted Manuscript version 2
21 Aug 2019 Author responded Author comments - Dan Li
Resubmission - Version 3
21 Aug 2019 Submitted Manuscript version 3
20 Sep 2019 Author responded Author comments - Dan Li
Resubmission - Version 4
20 Sep 2019 Submitted Manuscript version 4
Publishing
25 Sep 2019 Editorially accepted
7 Nov 2019 Article published 10.1186/s12881-019-0897-5

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