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Peer Review reports

From: De novoframeshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies

Original Submission
13 Jun 2013 Submitted Original manuscript
29 Jul 2013 Reviewed Reviewer Report - EC Tan
2 Aug 2013 Reviewed Reviewer Report - Zubair Ahmed
10 Aug 2013 Reviewed Reviewer Report - Yong-hui Jiang
23 Aug 2013 Author responded Author comments - Darrell Dinwiddie
Resubmission - Version 2
23 Aug 2013 Submitted Manuscript version 2
Publishing
11 Sep 2013 Editorially accepted
17 Sep 2013 Article published 10.1186/1755-8794-6-32

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