The additional genetic diagnosis of homozygous sickle cell disease in a patient with Waardenburg-Shah syndrome: a case report
Pre-publication versions of this article are available by contacting email@example.com.
|21 Sep 2018||Submitted||Original manuscript|
|7 Oct 2018||Reviewed||Reviewer Report - PAVANKUMAR TANDRA|
|9 Oct 2018||Reviewed||Reviewer Report - Umit Yavuz Malkan|
|4 Nov 2018||Reviewed||Reviewer Report - aisha alosail|
|3 Dec 2018||Author responded||Author comments - Angela Edna Rankine-Mullings|
|Resubmission - Version 2|
|3 Dec 2018||Submitted||Manuscript version 2|
|4 Dec 2018||Reviewed||Reviewer Report - Umit Yavuz Malkan|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|12 Dec 2018||Editorially accepted|
|13 Jan 2019||Article published||10.1186/s13256-018-1953-z|
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