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Peer Review reports

From: Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report

Original Submission
3 Jul 2014 Submitted Original manuscript
4 Aug 2014 Reviewed Reviewer Report - Giovanni Neri
2 Oct 2014 Reviewed Reviewer Report - Pietro Chiurazzi
24 Oct 2014 Author responded Author comments - Ranhui Duan
Resubmission - Version 2
24 Oct 2014 Submitted Manuscript version 2
2 Nov 2014 Author responded Author comments - Ranhui Duan
Resubmission - Version 3
2 Nov 2014 Submitted Manuscript version 3
Publishing
4 Nov 2014 Editorially accepted
25 Nov 2014 Article published 10.1186/s12881-014-0125-2

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