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Peer Review reports

From: The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz Syndrome

Original Submission
10 Nov 2015 Submitted Original manuscript
20 Nov 2015 Reviewed Reviewer Report - Filippo M. Santorelli
30 Nov 2015 Reviewed Reviewer Report - MaBgorzata J.M. Nowaczyk
4 Dec 2015 Author responded Author comments - Arianna Tucci
Resubmission - Version 2
4 Dec 2015 Submitted Manuscript version 2
Publishing
9 Mar 2016 Editorially accepted
11 Mar 2016 Article published 10.1186/s12881-016-0287-1

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