Showing 1 - 5 results of 5 for search 'McGuire, K', query time: 0.03s
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Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples by Thomson, K, Watkins, H, Farrall, M, Taylor, J, Walsh, R, Ware, J, Funke, B, Woodley, J, McGuire, K, Mazzarotto, F, Blair, E, Seller, A, Minikel, E, Exome Aggregation Consortium, MacArthur, D, Cook, S
Published 2016Journal article -
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A Re-evaluation of the South Asian MYBPC3Δ25 Intronic Deletion in Hypertrophic Cardiomyopathy by Harper, AR, Bowman, M, Hayesmoore, JBG, Sage, H, Salatino, S, Blair, E, Campbell, C, Currie, B, Goel, A, McGuire, K, Ormondroyd, E, Sergeant, K, Waring, A, Woodley, J, Kramer, CM, Neubauer, S, Farrall, M, Watkins, H, Thomson, KL
Published 2020Journal article -
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Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield by Thomson, K, Ormondroyd, E, Harper, A, Dent, T, McGuire, K, Baksi, J, Blair, E, Brennan, P, Buchan, R, Bueser, T, Campbell, C, Carr-White, G, Cook, S, Daniels, M, Deevi, S, Goodship, J, Hayesmoore, J, Henderson, A, Lamb, T, Prasad, S, Rayner-Matthews, P, Robert, L, Sneddon, L, Stark, H, Walsh, R, Ware, J, Farrall, M, Watkins, H, Nihr Bioresource – Rare Diseases Consortium
Published 2018Journal article