Peer Review reports
From: An inherited FGFR2 mutation increased osteogenesis gene expression and result in Crouzon syndrome
| Original Submission | ||
|---|---|---|
| 10 Jan 2018 | Submitted | Original manuscript |
| 3 Feb 2018 | Reviewed | Reviewer Report - Ozgul Alper |
| 17 Mar 2018 | Reviewed | Reviewer Report - Vivek Shukla |
| 2 Apr 2018 | Author responded | Author comments - Xianqun Fan |
| Resubmission - Version 2 | ||
| 2 Apr 2018 | Submitted | Manuscript version 2 |
| 6 May 2018 | Author responded | Author comments - Xianqun Fan |
| Resubmission - Version 3 | ||
| 6 May 2018 | Submitted | Manuscript version 3 |
| 13 May 2018 | Author responded | Author comments - Xianqun Fan |
| Resubmission - Version 4 | ||
| 13 May 2018 | Submitted | Manuscript version 4 |
| Publishing | ||
| 18 May 2018 | Editorially accepted | |
| 30 May 2018 | Article published | 10.1186/s12881-018-0607-8 |
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