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Peer Review reports

From: Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

Original Submission
10 Mar 2011 Submitted Original manuscript
2 May 2011 Reviewed Reviewer Report - Dana Crawford
4 Jun 2011 Reviewed Reviewer Report - Sintia Belangero
8 Jul 2011 Author responded Author comments - Yuejuan Xu
Resubmission - Version 2
8 Jul 2011 Submitted Manuscript version 2
28 Jul 2011 Reviewed Reviewer Report - Dana Crawford
3 Sep 2011 Author responded Author comments - Yuejuan Xu
Resubmission - Version 3
3 Sep 2011 Submitted Manuscript version 3
23 Sep 2011 Reviewed Reviewer Report - Dana Crawford
12 Nov 2011 Author responded Author comments - Yuejuan Xu
Resubmission - Version 4
12 Nov 2011 Submitted Manuscript version 4
20 Nov 2011 Reviewed Reviewer Report - Dana Crawford
23 Nov 2011 Author responded Author comments - Yuejuan Xu
Resubmission - Version 5
23 Nov 2011 Submitted Manuscript version 5
17 Dec 2011 Author responded Author comments - Yuejuan Xu
Resubmission - Version 6
17 Dec 2011 Submitted Manuscript version 6
Publishing
21 Dec 2011 Editorially accepted
21 Dec 2011 Article published 10.1186/1471-2350-12-169

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