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Identification of a rare 17p13.3 duplication including the BHLHA9 and YWHAEgenes in a family with developmental delay and behavioural problems

  • Valeria Capra1,
  • Marisol Mirabelli-Badenier2,
  • Michela Stagnaro2,
  • Andrea Rossi3,
  • Elisa Tassano5,
  • Stefania Gimelli4 and
  • Giorgio Gimelli5Email author
Contributed equally
BMC Medical Genetics201213:93

DOI: 10.1186/1471-2350-13-93

Received: 21 March 2012

Accepted: 1 October 2012

Published: 4 October 2012

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Open Peer Review reports

Pre-publication versions of this article and author comments to reviewers are available by contacting info@biomedcentral.com.

Original Submission
21 Mar 2012 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
17 May 2012 Author responded Author comments - Giorgio Gimelli
Resubmission - Version 3
17 May 2012 Submitted Manuscript version 3
28 Jun 2012 Reviewed Reviewer Report - Damien Bruno
28 Jun 2012 Reviewed Reviewer Report - Roberto Ravazzolo
3 Aug 2012 Author responded Author comments - Giorgio Gimelli
Resubmission - Version 4
3 Aug 2012 Submitted Manuscript version 4
13 Aug 2012 Reviewed Reviewer Report - Roberto Ravazzolo
22 Aug 2012 Reviewed Reviewer Report - Damien Bruno
10 Sep 2012 Author responded Author comments - Giorgio Gimelli
Resubmission - Version 5
10 Sep 2012 Submitted Manuscript version 5
23 Sep 2012 Reviewed Reviewer Report - Damien Bruno
Resubmission - Version 6
Submitted Manuscript version 6
Publishing
1 Oct 2012 Editorially accepted
4 Oct 2012 Article published 10.1186/1471-2350-13-93

How does Open Peer Review work?

Open peer review is a system where authors know who the reviewers are, and the reviewers know who the authors are. If the manuscript is accepted, the named reviewer reports are published alongside the article. Pre-publication versions of the article and author comments to reviewers are available by contacting info@biomedcentral.com. All previous versions of the manuscript and all author responses to the reviewers are also available.

You can find further information about the peer review system here.

Authors’ Affiliations

(1)
U.O. Neurochirurgia, Istituto G.Gaslini
(2)
U.O. Neuropsichiatria, Istituto G.Gaslini
(3)
Dipartimento di Neuroradiologia, Istituto G. Gaslini
(4)
Service of Genetic Medicine, University Hospitals of Geneva
(5)
Laboratorio di Citogenetica, Istituto G. Gaslini

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