TEMPERATURE-CONTROLLED PEDESTAL FOR SEMICONDUCTOR WAFER PROCESSING von BOURDON, Norman M, FENG, Jingbin, STRENG, Bradley Taylor, DURBIN, Aaron

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Finding diagnostically useful patterns in quantitative phenotypic data von Aitken, S, Kini, U, Parker, MJ, Sarkar, A, Joss, S, McKee, S, Scott, RH, Hurles, ME, FitzPatrick, DR, Fitzgerald, TW, van Kogelenberg, M, Morley, KI, Barrett, DM, Bayzetinova, T, Gribble, S, Middleton, A, Miller, R, Rajan, D, Akawi, N, Andrews, R, Anjum, U, Archer, H, Banerjee, R, Barelle, D, Batstone, P, Blair, E, Blyth, M, Brady, A, Bumpstead, SJ, Burn, J, Burton, J, Chandler, K, Clayton-Smith, J, Cooper, N, Cresswell, L, Crow, Y, Dabir, T, Davies, S, Deshpande, C, Devlin, G, Donnelly, C, Donnelly, D, Fisher, R, Pereira, SLG, Goodship, J, Goudie, D, Gray, E, Hawkins, R, Holder, S, Hollingsworth, G, Homfray, T, Irving, M, Jarvis, J, Jones, D, Jones, E, Josifova, D, Kazembe, S, Kerr, B, Kirk, C, Lam, W, Maher, E, Mansour, S, Maye, U, McCann, E, McGowan, R, McMullan, DJ, Metcalfe, K, Morris, A, Nevitt, L, Newbury-Ecob, R, Norman, A, Park, S, Porteous, D, Proctor, A, Purnell, H, Ragge, N, Rice, D, Roberts, G, Roberts, J, Ross, A, Sandford, R, Schweiger, S, Selby, A, Seller, A, Sharif, S, Shears, D, Simonic, I, Smith, B, Squires, M, Stewart, H, Sweeney, E, Taylor, R, Temple, IK, Treacy, B, Turnpenny, P, Tysoe, C, Whiteford, M, Williams, D, Yang, F, Parker, M

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Prevalence and architecture of de novo mutations in developmental disorders von Clayton, S, Sifrim, A, Ambridge, K, Barrett, DM, Krishnappa, N, Singh, T, Anjum, U, Archer, H, Baralle, D, Barnicoat, A, Baty, D, Berg, J, Bohanna, D, Bourn, D, Brunstrom, K, Canham, N, Castle, B, Chatzimichali, E, Cole, T, Colgiu, I, Collins, A, Collinson, MN, Cooper, N, Crow, Y, Davidson, R, Dean, J, Donnai, D, Donnelly, C, Douglas, A, Everest, S, Fendick, T, Ghali, N, Goudie, D, Green, A, Gribble, S, Hawkins, R, Henderson, A, Hewitt, S, Holder, S, Homfray, T, Islam, L, Jackson, A, Kazembe, S, Kini, U, Kirby, G, Kivuva, E, Lachlan, K, Langman, C, Lees, M, Lim, D, Lowther, G, Lynch, SA, Mansour, S, Marks, K, Maye, U, McCann, E, McMullan, DJ, McWilliam, C, Miles, E, Mohammed, S, Morgan, S, Mugalaasi, H, Naik, S, Nevitt, L, Norman, A, O'Shea, R, Ogilvie, C, Ong, K-R, Patel, C, Roberts, E, Samant, S, Sarkar, A, Scott, R, Scurr, I, Sequeira, C, Shannon, N, Shearing, E, Shears, D, Sneddon, L, Squires, M, Stewart, F, Suri, M, Sutton, V, Tatton-Brown, K, Thomson, J, Tomkins, S, Tysoe, C, Varghese, V, Vogt, J, Waters, J, Weber, A, Widaa, S, Wilcox, S, Williams, N, Woods, G, Wright, M, Yates, L, Yau, M, Nellaker, C, Barrett, JC

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Prevalence and architecture of de novo mutations in developmental disorders von Clayton, S, Sifrim, A, Ambridge, K, Barrett, DM, Krishnappa, N, Singh, T, Anjum, U, Archer, H, Baralle, D, Barnicoat, A, Baty, D, Berg, J, Bohanna, D, Bourn, D, Brunstrom, K, Canham, N, Castle, B, Chatzimichali, E, Cole, T, Colgiu, I, Collins, A, Collinson, MN, Cooper, N, Crow, Y, D’Alessandro, M, Davidson, R, Dean, J, Donnai, D, Donnelly, C, Douglas, A, Everest, S, Fendick, T, Ghali, N, Goudie, D, Green, A, Gribble, S, Hawkins, R, Henderson, A, Hewitt, S, Holder, S, Homfray, T, Islam, L, Jackson, A, Kazembe, S, Kini, U, Kirby, G, Kivuva, E, Lachlan, K, Langman, C, Lees, M, Lim, D, Lowther, G, Lynch, SA, Mansour, S, Marks, K, Maye, U, McCann, E, McMullan, DJ, McWilliam, C, Miles, E, Mohammed, S, Morgan, S, Mugalaasi, H, Naik, S, Nevitt, L, Norman, A, Ogilvie, C, Ong, K-R, Patel, C, Roberts, E, Samant, S, Sarkar, A, Scott, R, Scurr, I, Sequeira, C, Shannon, N, Shearing, E, Shears, D, Sneddon, L, Squires, M, Stewart, F, Suri, M, Sutton, V, Tatton-Brown, K, Temple, IK, Thomson, J, Tomkins, S, Tysoe, C, Varghese, V, Vogt, J, Waters, J, Weber, A, Widaa, S, Wilcox, S, Williams, N, Woods, G, Wright, M, Yates, L, Yau, M, Barrett, JC

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Prevalence and architecture of de novo mutations in developmental disorders von Clayton, S, Sifrim, A, Barrett, D.M, Jones, W.D, Krishnappa, N, Singh, T, Anjum, U, Archer, H, Baralle, D, Barnicoat, A, Baty, D, Berg, J, Bohanna, D, Bourn, D, Brunstrom, K, Canham, N, Castle, B, Chatzimichali, E, Cole, T, Colgiu, I, Collins, A, Collinson, M.N, Cooper, N, Crow, Y, Davidson, R, Dean, J, Donnai, D, Donnelly, C, Douglas, A, Everest, S, Fendick, T, Ghali, N, Goudie, D, Green, A, Hawkins, R, Henderson, A, Hewitt, S, Holder, S, Homfray, T, Islam, L, Jackson, A, Kazembe, S, Kini, U, Kirby, G, Kivuva, E, Kumar, V.K.A, Lachlan, K, Langman, C, Lees, M, Lim, D, Lowther, G, Mansour, S, Marks, K, Maye, U, McCann, E, McWilliam, C, Miles, E, Mohammed, S, Morgan, S, Mugalaasi, H, Naik, S, Nevitt, L, Norman, A, O'Shea, R, Ogilvie, C, Park, S.-M, Patel, C, Pilz, D.T, Roberts, E, Samant, S, Sarkar, A, Scott, R, Scurr, I, Sequeira, C, Shannon, N, Shearing, E, Shears, D, Sneddon, L, Squires, M, Stewart, F, Suri, M, Sutton, V, Tatton-Brown, K, Thomson, J, Tomkins, S, Tysoe, C, Varghese, V, Vogt, J, Waters, J, Weber, A, Widaa, S, Wilcox, S, Williams, N, Woods, G, Wright, M, Yates, L, Yau, M, Nellaker, C, FitzPatrick, D.R, Barrett, J.C

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Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study von Clayton, S, Sifrim, A, Alvi, M, Ambridge, K, Barrett, DM, Krishnappa, N, Singh, T, Anjum, U, Archer, H, Baralle, D, Barnicoat, A, Baty, D, Bennett, C, Berg, J, Bohanna, D, Bourn, D, Brunstrom, K, Canham, N, Castle, B, Chatzimichali, E, Cole, T, Colgiu, I, Collins, A, Collinson, MN, Cooper, N, Crow, Y, Davidson, R, Dean, J, Donnai, D, Donnelly, C, Douglas, A, Everest, S, Fendick, T, Ghali, N, Goudie, D, Green, A, Gribble, S, Harrison, V, Hawkins, R, Hellens, S, Henderson, A, Holder, S, Hollingsworth, G, Homfray, T, Ingram, S, Islam, L, Jenkins, L, Johnson, D, Joss, S, Kaemba, B, Kingston, H, Kini, U, Kirk, C, Kumar, VKA, Lampe, A, Lowther, G, Male, A, Mansour, S, Martin, K, McGowan, R, McKay, K, McWilliam, C, Metcalfe, K, Middleton, A, Miles, E, Murphy, H, Naik, S, Newbury-Ecob, R, O'Shea, R, Perrett, D, Phipps, J, Prescott, K, Quarrell, O, Rahbari, R, Randall, J, Raymond, L, Roberts, J, Ross, A, Saggar, A, Sarkar, A, Sequeira, C, Singzon, R, Skitt, Z, Smith, K, Smithson, S, Stewart, F, Stewart, H, Sweeney, E, Tatton-Brown, K, Tein, M, Tischkowitz, M, Tomkins, S, Torokwa, A, Varghese, V, Vogt, J, Wakeling, E, Wellesley, D, Wragg, C, Yau, M, FitzPatrick, DR

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Large-scale discovery of novel genetic causes of developmental disorders von Fitzgerald, T.W, Gerety, S.S, Jones, W.D, Al-Turki, S, Barrett, D.M, Gribble, S, Krishnappa, N, Middleton, A, Tivey, A.R, Andrews, R, Banerjee, R, Batstone, P, Blair, E, Blyth, M, Bohanna, D, Bourdon, L, Brady, A, Burn, J, Chandler, K, Clayton-Smith, J, Cole, T, Collinson, M.N, Cooper, N, Cresswell, L, Crow, Y, Davidson, R, Davies, S, Deshpande, C, Donnelly, C, Donnelly, D, Douglas, A, Elmslie, F, Ghali, N, Goudie, D, Gray, E, Hawkins, R, Holden, S, Holder, S, Hollingsworth, G, Homfray, T, Jarvis, J, Jones, D, Kinning, E, Kirk, C, Kivuva, E, Lam, W, Lampe, A, Langman, C, Lees, M, Lim, D, Lynch, S.A, Marks, K, Martin, K, McConnell, V, McEntagart, M, McKay, K, Metcalfe, K, Montgomery, T, Morgan, S, Morris, A, Morton, J, Mugalaasi, H, Murday, V, Nevitt, L, Newbury-Ecob, R, Norman, A, O'Shea, R, Parker, M.J, Paterson, J, Porteous, D, Prescott, K, Rice, D, Roberts, E, Roberts, J, Roberts, P, Rosser, E, Sandford, R, Seller, A, Shannon, N, Shaw-Smith, C, Simonic, I, Smithson, S, Splitt, M, Stewart, F, Stewart, H, Swaminathan, G.J, Taylor, C, Taylor, R, Turner, C, Tysoe, C, Vandersteen, A, Wakeling, E, Walker, D, Waters, J, Wellesley, D, Wragg, C, Yau, M, Carter, N.P, Firth, H.V, Hurles, M.E

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