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Peer Review reports

From: Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype

Original Submission
10 Jun 2013 Submitted Original manuscript
27 Jun 2013 Author responded Author comments - stefano stagi
Resubmission - Version 2
27 Jun 2013 Submitted Manuscript version 2
14 Oct 2013 Reviewed Reviewer Report - Fiorella Gurrieri
30 Nov 2013 Reviewed Reviewer Report - Fernando Scaglia
15 Jan 2014 Author responded Author comments - stefano stagi
Resubmission - Version 3
15 Jan 2014 Submitted Manuscript version 3
Publishing
23 Jan 2014 Editorially accepted
30 Jan 2014 Article published 10.1186/1471-2350-15-16

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BMC Medical Genetics

ISSN: 1471-2350

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