Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
© Talseth-Palmer et al.; licensee BioMed Central Ltd. 2013
Received: 27 August 2012
Accepted: 18 March 2013
Published: 26 March 2013
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|27 Aug 2012||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|19 Dec 2012||Reviewed||Reviewer Report - Xueling Sim|
|15 Jan 2013||Reviewed||Reviewer Report - Jiannis Ragoussis|
|6 Feb 2013||Author responded||Author comments - Bente Talseth-Palmer|
|Resubmission - Version 3|
|6 Feb 2013||Submitted||Manuscript version 3|
|24 Feb 2013||Reviewed||Reviewer Report - Xueling Sim|
|6 Mar 2013||Reviewed||Reviewer Report - Jiannis Ragoussis|
|15 Mar 2013||Author responded||Author comments - Bente Talseth-Palmer|
|Resubmission - Version 4|
|15 Mar 2013||Submitted||Manuscript version 4|
|17 Mar 2013||Author responded||Author comments - Bente Talseth-Palmer|
|Resubmission - Version 5|
|17 Mar 2013||Submitted||Manuscript version 5|
|18 Mar 2013||Editorially accepted|
|26 Mar 2013||Article published||10.1186/1755-8794-6-10|
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