Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients
© Zhao et al.; licensee BioMed Central Ltd. 2012
Received: 19 December 2011
Accepted: 20 June 2012
Published: 29 June 2012
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting firstname.lastname@example.org.
|19 Dec 2011||Submitted||Original manuscript|
|27 Jan 2012||Reviewed||Reviewer Report - Adam de Smith|
|21 Feb 2012||Reviewed||Reviewer Report - Melissa Wilson|
|11 Apr 2012||Author responded||Author comments - Linlu Zhao|
|Resubmission - Version 2|
|11 Apr 2012||Submitted||Manuscript version 2|
|3 May 2012||Reviewed||Reviewer Report - Adam de Smith|
|25 May 2012||Reviewed||Reviewer Report - Melissa Wilson|
|14 Jun 2012||Author responded||Author comments - Linlu Zhao|
|Resubmission - Version 3|
|14 Jun 2012||Submitted||Manuscript version 3|
|20 Jun 2012||Editorially accepted|
|29 Jun 2012||Article published||10.1186/1471-2393-12-61|
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