The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome
Pre-publication versions of this article 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|
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