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Peer Review reports

From: Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type

Original Submission
15 Dec 2010 Submitted Original manuscript
25 Jan 2011 Author responded Author comments - Lourdes Loidi
Resubmission - Version 2
25 Jan 2011 Submitted Manuscript version 2
6 Apr 2011 Reviewed Reviewer Report - ERik Imel
11 Apr 2011 Reviewed Reviewer Report - Yves Sabbagh
15 Jun 2011 Author responded Author comments - Lourdes Loidi
Resubmission - Version 3
15 Jun 2011 Submitted Manuscript version 3
28 Jun 2011 Reviewed Reviewer Report - Yves Sabbagh
3 Jul 2011 Reviewed Reviewer Report - ERik Imel
Resubmission - Version 4
Submitted Manuscript version 4
2 Aug 2011 Author responded Author comments - Lourdes Loidi
Resubmission - Version 5
2 Aug 2011 Submitted Manuscript version 5
14 Aug 2011 Reviewed Reviewer Report - ERik Imel
22 Aug 2011 Author responded Author comments - Lourdes Loidi
Resubmission - Version 6
22 Aug 2011 Submitted Manuscript version 6
30 Aug 2011 Author responded Author comments - Lourdes Loidi
Resubmission - Version 7
30 Aug 2011 Submitted Manuscript version 7
2 Sep 2011 Author responded Author comments - Lourdes Loidi
Resubmission - Version 8
2 Sep 2011 Submitted Manuscript version 8
Publishing
8 Sep 2011 Editorially accepted
8 Sep 2011 Article published 10.1186/1471-2350-12-116

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