This article has Open Peer Review reports available.
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform
- Sarah De Keulenaer1,
- Jan Hellemans1, 2,
- Steve Lefever2,
- Jean-Pierre Renard3,
- Joachim De Schrijver3,
- Hendrik Van de Voorde2,
- Mohammad Amin Tabatabaiefar5, 6,
- Filip Van Nieuwerburgh1, 4,
- Daisy Flamez1, 3,
- Filip Pattyn2,
- Bieke Scharlaken1,
- Dieter Deforce1, 4,
- Sofie Bekaert1,
- Wim Van Criekinge1, 3,
- Jo Vandesompele1, 2,
- Guy Van Camp5 and
- Paul Coucke1, 2Email author
© De Keulenaer et al.; licensee BioMed Central Ltd. 2012
Received: 12 December 2011
Accepted: 7 May 2012
Published: 18 May 2012
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|12 Dec 2011||Submitted||Original manuscript|
|16 Mar 2012||Reviewed||Reviewer Report - Lisbeth Tranebjaerg|
|19 Mar 2012||Reviewed||Reviewer Report - Shin-ichi Usami|
|27 Apr 2012||Author responded||Author comments - Sarah De Keulenaer|
|Resubmission - Version 2|
|27 Apr 2012||Submitted||Manuscript version 2|
|7 May 2012||Editorially accepted|
|18 May 2012||Article published||10.1186/1755-8794-5-17|
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