This article has Open Peer Review reports available.
The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome
- Laura M McDonell†1,
- Jodi Warman Chardon†2,
- Jeremy Schwartzentruber3,
- Denise Foster4,
- Chandree L Beaulieu1,
- FORGE Canada Consortium1,
- Jacek Majewski5,
- Dennis E Bulman1, 6 and
- Kym M Boycott1, 2, 6Email author
© McDonell et al.; licensee BioMed Central Ltd. 2014
Received: 11 November 2013
Accepted: 22 January 2014
Published: 31 January 2014
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting firstname.lastname@example.org.
|11 Nov 2013||Submitted||Original manuscript|
|6 Dec 2013||Reviewed||Reviewer Report - Wasim Ahmad|
|10 Dec 2013||Reviewed||Reviewer Report - Bobby Koeleman|
|8 Jan 2014||Author responded||Author comments - Kym Boycott|
|Resubmission - Version 2|
|8 Jan 2014||Submitted||Manuscript version 2|
|17 Jan 2014||Author responded||Author comments - Kym Boycott|
|Resubmission - Version 3|
|17 Jan 2014||Submitted||Manuscript version 3|
|22 Jan 2014||Editorially accepted|
|31 Jan 2014||Article published||10.1186/1471-2377-14-22|
How does Open Peer Review work?
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 and author comments to reviewers are available by contacting email@example.com. All previous versions of the manuscript and all author responses to the reviewers are also available.
You can find further information about the peer review system here.