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Peer Review reports

From: Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiency

Original Submission
6 Nov 2013 Submitted Original manuscript
12 Nov 2013 Author responded Author comments - Daniel Lieber
Resubmission - Version 2
12 Nov 2013 Submitted Manuscript version 2
Resubmission - Version 3
Submitted Manuscript version 3
24 Dec 2013 Reviewed Reviewer Report - Gregory Enns
27 Dec 2013 Reviewed Reviewer Report - Jose Abdenur
20 Feb 2014 Author responded Author comments - Daniel Lieber
Resubmission - Version 4
20 Feb 2014 Submitted Manuscript version 4
Publishing
25 Feb 2014 Editorially accepted
6 Mar 2014 Article published 10.1186/1471-2350-15-30

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