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 |
14 Mar 2014 | Reviewed | Reviewer Report - david Dyment |
7 Apr 2014 | Author responded | Author comments - Carlos Lopez-Otin |
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 |