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Peer Review reports

From: A novel description of a syndrome consisting of 7q21.3 deletion including DYNC1I1 with preserved DLX5/6 without ectrodactyly: a case report

Original Submission
7 Oct 2015 Submitted Original manuscript
5 Feb 2016 Reviewed Reviewer Report - Devendra Sawant
5 Mar 2016 Reviewed Reviewer Report - Mavroudis Voultsos
8 Mar 2016 Author responded Author comments - Héctor Ramos-Zaldívar
Resubmission - Version 2
8 Mar 2016 Submitted Manuscript version 2
29 Apr 2016 Editorially accepted
13 Jun 2016 Article published 10.1186/s13256-016-0921-8

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