A novel description of a syndrome consisting of 7q21.3 deletion including DYNC1I1 with preserved DLX5/6 without ectrodactyly: a case report
Pre-publication versions of this article are available by contacting email@example.com.
|7 Oct 2015||Submitted||Original manuscript|
|5 Feb 2016||Reviewed||Reviewer Report - Devendra Sawant|
|5 Mar 2016||Reviewed||Reviewer Report - Mavroudis Voultsos|
|8 Mar 2016||Author responded||Author comments - Héctor Ramos-Zaldívar|
|Resubmission - Version 2|
|8 Mar 2016||Submitted||Manuscript version 2|
|29 Apr 2016||Editorially accepted|
|13 Jun 2016||Article published||10.1186/s13256-016-0921-8|
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