Skip to main content

Peer Review reports

From: Whole-exome sequencing identifies a novel mutation in spermine synthase gene (SMS) associated with Snyder-Robinson Syndrome

Original Submission
20 Apr 2020 Submitted Original manuscript
25 Apr 2020 Author responded Author comments - Talal J. Qazi
Resubmission - Version 2
25 Apr 2020 Submitted Manuscript version 2
17 May 2020 Reviewed Reviewer Report
21 May 2020 Reviewed Reviewer Report - Francesca Cogliati
17 Jun 2020 Author responded Author comments - Talal J. Qazi
Resubmission - Version 3
17 Jun 2020 Submitted Manuscript version 3
30 Jun 2020 Author responded Author comments - Talal J. Qazi
Resubmission - Version 4
30 Jun 2020 Submitted Manuscript version 4
8 Jul 2020 Author responded Author comments - Talal J. Qazi
Resubmission - Version 5
8 Jul 2020 Submitted Manuscript version 5
11 Jul 2020 Author responded Author comments - Talal J. Qazi
Resubmission - Version 6
11 Jul 2020 Submitted Manuscript version 6
17 Jul 2020 Author responded Author comments - Talal J. Qazi
Resubmission - Version 7
17 Jul 2020 Submitted Manuscript version 7
22 Jul 2020 Author responded Author comments - Talal J. Qazi
Resubmission - Version 8
22 Jul 2020 Submitted Manuscript version 8
Publishing
26 Jul 2020 Editorially accepted
24 Aug 2020 Article published 10.1186/s12881-020-01095-x

You can find further information about peer review here.

Back to article page