Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|23 Oct 2012||Submitted||Original manuscript|
|15 Nov 2012||Reviewed||Reviewer Report - Karen Usdin|
|4 Jan 2013||Reviewed||Reviewer Report - Hengmi Cui|
|18 Jan 2013||Author responded||Author comments - Stephen Warren|
|Resubmission - Version 2|
|18 Jan 2013||Submitted||Manuscript version 2|
|20 Jan 2013||Reviewed||Reviewer Report - Bo Wen|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|25 Jan 2013||Editorially accepted|
|29 Jan 2013||Article published||10.1186/1471-2350-14-18|
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