Research article
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
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