Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel
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Genome medicine - ISSN 1756-994X-16:1 (2024) p. 1-14
From silence to surge : illuminating the stealthy threat of aneurysms and dissections with the aid of cell models and insights into the genetic architecture
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Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2024,269 p.
Phenotypic spectrum of the first Belgian MYBPC3 founder : a large multi-exon deletion with a varying phenotype
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Frontiers in genetics - ISSN 1664-8021-15 (2024) p. 1-15
Variants in structural cardiac genes in patients with cancer therapy-related cardiac dysfunction after anthracycline chemotherapy : a case control study
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Cardio-Oncology - ISSN 2057-3804-10:1 (2024) p. 1-12
Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome
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Npj genomic medicine - ISSN 2056-7944-9:1 (2024) p. 1-9