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Peer Review reports

From: Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review

Original Submission
17 Jul 2017 Submitted Original manuscript
15 Aug 2017 Author responded Author comments - Li Tan
Resubmission - Version 2
15 Aug 2017 Submitted Manuscript version 2
22 Aug 2017 Author responded Author comments - Li Tan
Resubmission - Version 3
22 Aug 2017 Submitted Manuscript version 3
26 Sep 2017 Reviewed Reviewer Report - Barry Eng
10 Oct 2017 Reviewed Reviewer Report - Alejandro Estrada
19 Oct 2017 Author responded Author comments - Li Tan
Resubmission - Version 4
19 Oct 2017 Submitted Manuscript version 4
23 Oct 2017 Reviewed Reviewer Report - Alejandro Estrada
2 Nov 2017 Reviewed Reviewer Report - Barry Eng
7 Nov 2017 Author responded Author comments - Li Tan
Resubmission - Version 5
7 Nov 2017 Submitted Manuscript version 5
Publishing
14 Nov 2017 Editorially accepted
1 Dec 2017 Article published 10.1186/s12881-017-0501-9

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