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 are available by contacting email@example.com.
|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|
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