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Peer Review reports

From: Exome sequencing identifies a novel mutation in PIK3R1 as the cause of SHORT syndrome

Original Submission
8 Nov 2013 Submitted Original manuscript
7 Apr 2014 Author responded Author comments - Carlos Lopez-Otin
14 Mar 2014 Reviewed Reviewer Report - david Dyment
Resubmission - Version 2
7 Apr 2014 Submitted Manuscript version 2
22 Apr 2014 Author responded Author comments - Carlos Lopez-Otin
Resubmission - Version 3
22 Apr 2014 Submitted Manuscript version 3
Publishing
25 Apr 2014 Editorially accepted
2 May 2014 Article published 10.1186/1471-2350-15-51

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