Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature
Pre-publication versions of this article are available by contacting email@example.com.
|28 Feb 2017||Submitted||Original manuscript|
|8 Jul 2017||Reviewed||Reviewer Report - Rikke Christensen|
|1 Sep 2017||Reviewed||Reviewer Report - Lawrence T. Reiter|
|1 Sep 2017||Reviewed||Reviewer Report - Karin Buiting|
|25 Oct 2017||Author responded||Author comments - Cinthia Aguilera|
|Resubmission - Version 2|
|25 Oct 2017||Submitted||Manuscript version 2|
|27 Oct 2017||Reviewed||Reviewer Report - Karin Buiting|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|14 Nov 2017||Editorially accepted|
|21 Nov 2017||Article published||10.1186/s12881-017-0500-x|
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