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Peer Review reports

From: A de novo KMT2D mutation in a girl with Kabuki syndrome associated with endocrine symptoms: a case report

Original Submission
16 Dec 2017 Submitted Original manuscript
6 Jan 2018 Reviewed Reviewer Report - N Miyake
21 Mar 2018 Reviewed Reviewer Report - J Liu
4 Apr 2018 Author responded Author comments - JungEun Moon
Resubmission - Version 2
4 Apr 2018 Submitted Manuscript version 2
22 Apr 2018 Author responded Author comments - JungEun Moon
Resubmission - Version 3
22 Apr 2018 Submitted Manuscript version 3
8 May 2018 Author responded Author comments - JungEun Moon
Resubmission - Version 4
8 May 2018 Submitted Manuscript version 4
Publishing
15 May 2018 Editorially accepted
18 Jun 2018 Article published 10.1186/s12881-018-0606-9

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