Brittle cornea syndrome: current perspectives by Walkden A, Burkitt-Wright E, Au L

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Brittle cornea syndrome: current perspectives [Response to Letter] by Walkden A, Burkitt-Wright E, Au L

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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

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

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