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Peer Review reports

From: Targeted/exome sequencing identified mutations in ten Chinese patients diagnosed with Noonan syndrome and related disorders

Original Submission
15 Jun 2017 Submitted Original manuscript
7 Jul 2017 Reviewed Reviewer Report - Reuben Pengelly
4 Aug 2017 Author responded Author comments - Shanshan Xu
Resubmission - Version 2
4 Aug 2017 Submitted Manuscript version 2
13 Oct 2017 Author responded Author comments - Shanshan Xu
Resubmission - Version 3
13 Oct 2017 Submitted Manuscript version 3
17 Oct 2017 Author responded Author comments - Shanshan Xu
Resubmission - Version 4
17 Oct 2017 Submitted Manuscript version 4
Publishing
20 Oct 2017 Editorially accepted
30 Oct 2017 Article published 10.1186/s12920-017-0298-6

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