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Peer Review reports

From: Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina)

Original Submission
1 Jul 2005 Submitted Original manuscript
23 Dec 2005 Reviewed Reviewer Report - Giorgio Carlomagno
10 Jan 2006 Reviewed Reviewer Report - Hakan Kaya
8 Feb 2006 Author responded Author comments - Daniel Guerrier
Resubmission - Version 2
8 Feb 2006 Submitted Manuscript version 2
8 Feb 2006 Author responded Author comments - Daniel Guerrier
Resubmission - Version 3
8 Feb 2006 Submitted Manuscript version 3
22 Feb 2006 Author responded Author comments - Daniel Guerrier
Resubmission - Version 4
22 Feb 2006 Submitted Manuscript version 4
Publishing
23 Mar 2006 Editorially accepted
23 Mar 2006 Article published 10.1186/1477-5751-5-4

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