BMC Medical Genetics

official impact factor 2.44

Open Access Highly Access Pre-publication history

Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis

Alessandra Ferlini*, Matteo Bovolenta, Marcella Neri, Francesca Gualandi, Alessandra Balboni, Anton Yuryev, Fabrizio Salvi, Donato Gemmati, Alberto Liboni and Paolo Zamboni

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