Open Access Pre-publication history

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

Yue-Juan Xu, Jian Wang, Rang Xu, Peng-Jun Zhao, Xi-Ke Wang, Heng-Juan Sun, Li-Ming Bao, Jie Shen, Qi-Hua Fu, Fen Li and Kun Sun*

BMC Medical Genetics 2011, 12:169  doi:10.1186/1471-2350-12-169

Pre-publication versions of this article and reviewers' reports

Original Submission - Version 1 Manuscript 10 Mar 2011
Reviewer's Report Dana Crawford 02 May 2011
Reviewer's Report Sintia Belangero 04 Jun 2011
Resubmission - Version 2 Manuscript Author's comment 08 Jul 2011
Reviewer's Report Dana Crawford 28 Jul 2011
Resubmission - Version 3 Manuscript Author's comment 03 Sep 2011
Reviewer's Report Dana Crawford 23 Sep 2011
Resubmission - Version 4 Manuscript Author's comment 12 Nov 2011
Resubmission - Version 5 Manuscript Author's comment 23 Nov 2011
Editorial acceptance 12 Dec 2011
Published 21 Dec 2011