Full text 2026 Genome Sequencing Readily Detects a Copy Number Variant in <i>FBN1</i> in a Patient with Marfan Syndrome Jean F, Stuart A, Care4Rare Canada Consortium, et al. Structural Variants Full text Loading PDF… Expand reader Download Abstract No abstract available. Keywords Genome sequencing Marfan syndrome Fbn1 Copy Number Variation Diagnostic Odyssey Care4rare Solve