Exome sequencing helped the fine diagnosis of two siblings afflicted with atypical Timothy syndrome (TS2)
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|12 Jun 2013||Submitted||Original manuscript|
|18 Jun 2013||Author responded||Author comments - Sebastian Froehler|
|Resubmission - Version 2|
|18 Jun 2013||Submitted||Manuscript version 2|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|6 Dec 2013||Reviewed||Reviewer Report - Jill Johnsen|
|19 Dec 2013||Reviewed||Reviewer Report - Jacob Tfelt-Hansen|
|13 Mar 2014||Author responded||Author comments - Sebastian Froehler|
|Resubmission - Version 4|
|13 Mar 2014||Submitted||Manuscript version 4|
|25 Apr 2014||Editorially accepted|
|29 Apr 2014||Article published||10.1186/1471-2350-15-48|
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