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This article has Open Peer Review reports available.

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De novo deletion of chromosome 11q12.3 in monozygotic twins affected by Poland Syndrome

  • Carlotta Maria Vaccari1,
  • Maria Victoria Romanini2,
  • Ilaria Musante1,
  • Elisa Tassano3,
  • Stefania Gimelli4,
  • Maria Teresa Divizia3,
  • Michele Torre5,
  • Carmen Gloria Morovic6,
  • Margherita Lerone3,
  • Roberto Ravazzolo1, 3, 7 and
  • Aldamaria Puliti1, 3, 7Email author
Contributed equally
BMC Medical Genetics201415:63

DOI: 10.1186/1471-2350-15-63

Received: 30 October 2013

Accepted: 23 May 2014

Published: 30 May 2014

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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
30 Oct 2013 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
25 Nov 2013 Reviewed Reviewer Report - Halil Ibrahim Atasoy
21 Jan 2014 Reviewed Reviewer Report - Anwar Baban
24 Mar 2014 Author responded Author comments - Aldamaria Puliti
Resubmission - Version 3
24 Mar 2014 Submitted Manuscript version 3
Resubmission - Version 4
Submitted Manuscript version 4
23 Apr 2014 Reviewed Reviewer Report - Halil Ibrahim Atasoy
10 May 2014 Author responded Author comments - Aldamaria Puliti
Resubmission - Version 5
10 May 2014 Submitted Manuscript version 5
22 May 2014 Author responded Author comments - Aldamaria Puliti
Resubmission - Version 6
22 May 2014 Submitted Manuscript version 6
Publishing
23 May 2014 Editorially accepted
30 May 2014 Article published 10.1186/1471-2350-15-63

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)
Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genoa
(2)
Plastic and Reconstructive Surgery Unit, IST - San Martino Hospital and University of Genoa
(3)
Medical Genetics Unit, Istituto Giannina Gaslini
(4)
Service of Genetic Medicine, University Hospitals of Geneva
(5)
Pediatric Surgery Unit, Istituto Giannina Gaslini
(6)
Pediatric Plastic Surgery Unit, Dr. Luis Calvo Mackenna Hospital
(7)
CEBR, University of Genoa

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