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Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline. by Giannoulatou, E, McVean, G, Taylor, I, McGowan, S, Maher, G, Iqbal, Z, Pfeifer, S, Turner, I, Burkitt Wright, E, Shorto, J, Itani, A, Turner, K, Gregory, L, Buck, D, Rajpert-De Meyts, E, Looijenga, L, Kerr, B, Wilkie, A, Goriely, A
Published 2013Journal article -
2
Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome by Pagnamenta, A, Kaisaki, P, Bennett, F, Burkitt-Wright, E, Martin, H, Ferla, M, Taylor, J, Gompertz, L, Lahiri, N, Tatton-Brown, K, Newbury-Ecob, R, Henderson, A, Joss, S, Weber, A, Carmichael, J, Turnpenny, P, McKee, S, Forzano, F, Ashraf, T, Bradbury, K, Shears, D, Kini, U, De Burca, A, The DDD Study, Blair, E, Taylor, J, Stewart, H
Published 2019Journal article -
3
The Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathway. by Stevenson, DA, Schill, L, Schoyer, L, Andresen, BS, Bakker, A, Bayrak-Toydemir, P, Burkitt-Wright, E, Chatfield, K, Elefteriou, F, Elgersma, Y, Fisher, MJ, Franz, D, Gelb, BD, Goriely, A, Gripp, KW, Hardan, AY, Keppler-Noreuil, KM, Kerr, B, Korf, B, Leoni, C, McCormick, F, Plotkin, SR, Rauen, KA, Reilly, K, Roberts, A, Sandler, A, Siegel, D, Walsh, K, Widemann, BC
Published 2016Journal article