Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform
Pre-publication versions of this article 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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Open peer review is a system where authors know who the reviewers are, and the reviewers know who the authors are. If the manuscript is accepted, the named reviewer reports are published alongside the article. Pre-publication versions of the article are available by contacting firstname.lastname@example.org.
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