De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|13 Jun 2013||Submitted||Original manuscript|
|29 Jul 2013||Reviewed||Reviewer Report - EC Tan|
|2 Aug 2013||Reviewed||Reviewer Report - Zubair Ahmed|
|10 Aug 2013||Reviewed||Reviewer Report - Yong-hui Jiang|
|23 Aug 2013||Author responded||Author comments - Darrell Dinwiddie|
|Resubmission - Version 2|
|23 Aug 2013||Submitted||Manuscript version 2|
|11 Sep 2013||Editorially accepted|
|17 Sep 2013||Article published||10.1186/1755-8794-6-32|
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