Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis
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* Corresponding author: Alessandra Ferlini fla@unife.it
BMC Medical Genetics 2010, 11:64 doi:10.1186/1471-2350-11-64
Pre-publication versions of this article and reviewers' reports
| Original Submission - Version 1 | Manuscript | 01 Aug 2009 | |
| Reviewer's Report | Sreeram Ramagopalan | 28 Aug 2009 | |
| Reviewer's Report | Manuel Comabella | 15 Sep 2009 | |
| Resubmission - Version 2 | Manuscript | Author's comment | 04 Dec 2009 |
| Reviewer's Report | Sreeram Ramagopalan | 22 Dec 2009 | |
| Reviewer's Report | Manuel Comabella | 13 Jan 2010 | |
| Resubmission - Version 3 | Manuscript | Author's comment | 19 Feb 2010 |
| Resubmission - Version 4 | Manuscript | Author's comment | 09 Mar 2010 |
| Editorial acceptance | 28 Mar 2010 | ||
| Published | 28 Apr 2010 |