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Peer Review reports

From: Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication

Original Submission
3 May 2016 Submitted Original manuscript
18 Aug 2016 Reviewed Reviewer Report - Santhosh Girirajan
22 Sep 2016 Reviewed Reviewer Report - Patricia Maciel
27 Sep 2016 Author responded Author comments - Jila Dastan
Resubmission - Version 2
27 Sep 2016 Submitted Manuscript version 2
29 Sep 2016 Author responded Author comments - Jila Dastan
Resubmission - Version 3
29 Sep 2016 Submitted Manuscript version 3
Publishing
20 Oct 2016 Editorially accepted
10 Nov 2016 Article published 10.1186/s12881-016-0340-0

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