Molecular analysis of exon 7 of the fibroblast growth factor receptor 2 ( FGFR2 ) gene in an Indonesian patient with Apert syndrome: a case report
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|6 Mar 2018||Submitted||Original manuscript|
|30 Apr 2018||Reviewed||Reviewer Report - Walid AL ACHKAR|
|18 Aug 2018||Reviewed||Reviewer Report - Adriano Alberti|
|27 Nov 2018||Reviewed||Reviewer Report - Nikhil Moorchung|
|4 Dec 2018||Reviewed||Reviewer Report - Satomi Okano|
|24 Jan 2019||Author responded||Author comments - Gara Samara Brajadenta|
|Resubmission - Version 2|
|24 Jan 2019||Submitted||Manuscript version 2|
|25 Apr 2019||Reviewed||Reviewer Report - Satomi Okano|
|30 Apr 2019||Reviewed||Reviewer Report - Adriano Alberti|
|6 May 2019||Reviewed||Reviewer Report - Nikhil Moorchung|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|24 Jun 2019||Editorially accepted|
|7 Aug 2019||Article published||10.1186/s13256-019-2173-x|
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