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Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
German Competence Network for Congenital Heart Defects, Oct 2021, In: Genetics in medicine. 23, 10, p. 1952-1960 9 p.Research output: Contribution to journal › Article* › Academic › peer-review
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Improving risk prediction in hypertrophic cardiomyopathy: the key role of Dutch founder variants
Walsh, R. & Pinto, Y. M., Jun 2021, In: Netherlands heart journal. 29, 6, p. 299-300 2 p.Research output: Contribution to journal › Comment/Letter to the editor* › Academic
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Desmin variants in cardiomyopathies – the hard yards in defining pathogenicity
Walsh, R., 15 May 2021, In: International journal of cardiology. 331, p. 208-209 2 p.Research output: Contribution to journal › Editorial* › Academic › peer-review
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