Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1locus
- Reid S Alisch†2, 5,
- Tao Wang†1, 2,
- Pankaj Chopra2,
- Jeannie Visootsak2, 4,
- Karen N Conneely2 and
- Stephen T Warren2, 3, 4Email author
© Alisch et al.; licensee BioMed Central Ltd. 2013
Received: 23 October 2012
Accepted: 25 January 2013
Published: 29 January 2013
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers 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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