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Peer Review reports

From: Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in pendred syndrome/enlarged vestibular aqueducts

Original Submission
2 Jan 2013 Submitted Original manuscript
16 May 2013 Reviewed Reviewer Report - Pu Dai
17 May 2013 Reviewed Reviewer Report - Lisbeth Tranebjaerg
23 May 2013 Reviewed Reviewer Report - Fiona Macdonald
18 Jul 2013 Author responded Author comments - Priya Landa
Resubmission - Version 2
18 Jul 2013 Submitted Manuscript version 2
21 Jul 2013 Reviewed Reviewer Report - Lisbeth Tranebjaerg
24 Jul 2013 Reviewed Reviewer Report - Pu Dai
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
6 Aug 2013 Editorially accepted
21 Aug 2013 Article published 10.1186/1471-2350-14-85

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BMC Medical Genetics

ISSN: 1471-2350

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