Severe persistent pulmonary hypertension of the newborn and dysmorphic features in neonate with a deletion involving TWIST1 and PHF14: a case report
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|13 Mar 2017||Submitted||Original manuscript|
|13 Apr 2017||Reviewed||Reviewer Report - Harith Baharith|
|20 Jul 2017||Author responded||Author comments - Carina Schinagl|
|Resubmission - Version 2|
|20 Jul 2017||Submitted||Manuscript version 2|
|23 Jul 2017||Editorially accepted|
|17 Aug 2017||Article published||10.1186/s13256-017-1402-4|
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