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Peer Review reports

From: Absence of mutations in NR2E1 and SNX3in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes

Original Submission
13 Feb 2007 Submitted Original manuscript
7 Mar 2007 Reviewed Reviewer Report - Uta Francke
16 Mar 2007 Reviewed Reviewer Report - Annick Raas-Rothschild
26 Mar 2007 Reviewed Reviewer Report - Maria Giuseppina Miano
29 Mar 2007 Reviewed Reviewer Report - Diane Cox
2 May 2007 Author responded Author comments - Elizabeth M Simpson
Resubmission - Version 2
2 May 2007 Submitted Manuscript version 2
19 May 2007 Reviewed Reviewer Report - Uta Francke
28 May 2007 Reviewed Reviewer Report - Maria Giuseppina Miano
29 May 2007 Reviewed Reviewer Report - Diane Cox
6 Jun 2007 Reviewed Reviewer Report - Annick Raas-Rothschild
28 Jun 2007 Author responded Author comments - Elizabeth M Simpson
Resubmission - Version 3
28 Jun 2007 Submitted Manuscript version 3
20 Jul 2007 Author responded Author comments - Elizabeth M Simpson
Resubmission - Version 4
20 Jul 2007 Submitted Manuscript version 4
20 Jul 2007 Author responded Author comments - Elizabeth M Simpson
Resubmission - Version 5
20 Jul 2007 Submitted Manuscript version 5
Publishing
26 Jul 2007 Editorially accepted
26 Jul 2007 Article published 10.1186/1471-2350-8-48

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