Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.
Skip to main content

Peer Review reports

From: A novel mutation in the WFS1gene identified in a Taiwanese family with low-frequency hearing impairment

Original Submission
28 Sep 2006 Submitted Original manuscript
13 Nov 2006 Reviewed Reviewer Report - Marci Lesperance
21 Nov 2006 Reviewed Reviewer Report - Lisbeth Tranebjaerg
25 Jan 2007 Author responded Author comments - Hsun-Tien Tsai
Resubmission - Version 2
25 Jan 2007 Submitted Manuscript version 2
8 Mar 2007 Reviewed Reviewer Report - Marci Lesperance
15 Mar 2007 Reviewed Reviewer Report - Lisbeth Tranebjaerg
7 May 2007 Author responded Author comments - Hsun-Tien Tsai
Resubmission - Version 3
7 May 2007 Submitted Manuscript version 3
16 May 2007 Author responded Author comments - Hsun-Tien Tsai
Resubmission - Version 4
16 May 2007 Submitted Manuscript version 4
Publishing
22 May 2007 Editorially accepted
22 May 2007 Article published 10.1186/1471-2350-8-26

You can find further information about peer review here.

Back to article page

BMC Medical Genetics

ISSN: 1471-2350

Contact us