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Expansion of a diagnostic service for hypertrophic cardiomyopathy using next generation sequencing Yazar: Reid, S, Woodley, J, Kaur, K, Thomson, K, Broxholme, J, Taylor, J, Blair, E, Taylor, J, Watkins, H
Baskı/Yayın Bilgisi 2011Conference item -
2
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples Yazar: 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
Baskı/Yayın Bilgisi 2016Journal article -
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A Re-evaluation of the South Asian MYBPC3Δ25 Intronic Deletion in Hypertrophic Cardiomyopathy Yazar: 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
Baskı/Yayın Bilgisi 2020Journal article