A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathy
© Hinkes et al.; licensee BioMed Central Ltd. 2012
Received: 9 November 2011
Accepted: 14 May 2012
Published: 14 May 2012
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|9 Nov 2011||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|18 Feb 2012||Reviewed||Reviewer Report - Sau Cheung|
|20 Mar 2012||Author responded||Author comments - Bernward Hinkes|
|Resubmission - Version 4|
|20 Mar 2012||Submitted||Manuscript version 4|
|14 May 2012||Editorially accepted|
|14 May 2012||Article published||10.1186/1471-2369-13-27|
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