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Peer Review reports

From: A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome

Original Submission
25 May 2011 Submitted Original manuscript
19 Jul 2011 Reviewed Reviewer Report - Masaru Katoh
Resubmission - Version 2
Submitted Manuscript version 2
23 Sep 2011 Editorially accepted
23 Sep 2011 Article published 10.1186/1471-2350-12-122

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