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Peer Review reports

From: Identification of a novel de novo mutation in the NIPBL gene in an Iranian patient with Cornelia de Lange syndrome: A case report

Original Submission
8 Feb 2010 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
Resubmission - Version 3
Submitted Manuscript version 3
Resubmission - Version 4
Submitted Manuscript version 4
29 Mar 2010 Reviewed Reviewer Report - I Barisic
19 Jul 2010 Author responded Author comments - Hamid Galehdari
Resubmission - Version 5
19 Jul 2010 Submitted Manuscript version 5
Resubmission - Version 6
Submitted Manuscript version 6
Resubmission - Version 7
Submitted Manuscript version 7
13 Nov 2010 Reviewed Reviewer Report - Matt Deardorff
30 Nov 2010 Author responded Author comments - Hamid Galehdari
Resubmission - Version 8
30 Nov 2010 Submitted Manuscript version 8
3 Dec 2010 Author responded Author comments - Hamid Galehdari
Resubmission - Version 9
3 Dec 2010 Submitted Manuscript version 9
4 Dec 2010 Author responded Author comments - Hamid Galehdari
Resubmission - Version 10
4 Dec 2010 Submitted Manuscript version 10
Publishing
27 Jun 2011 Editorially accepted
27 Jun 2011 Article published 10.1186/1752-1947-5-242

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