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Results: 1-14 |
Results: 14

Authors: Dye, D Stone, HJ Reed, RC
Citation: D. Dye et al., A two phase elastic-plastic self-consistent model for the accumulation of microstrains in Waspaloy, ACT MATER, 49(7), 2001, pp. 1271-1283

Authors: Dye, D Hunziker, O Reed, RC
Citation: D. Dye et al., Numerical analysis of the weldability of superalloys, ACT MATER, 49(4), 2001, pp. 683-697

Authors: Dye, D Stone, HJ Reed, RC
Citation: D. Dye et al., Intergranular and interphase microstresses, CURR OP SOL, 5(1), 2001, pp. 31-37

Authors: Dye, D Hunziker, O Roberts, SM Reed, RC
Citation: D. Dye et al., Modeling of the mechanical effects induced by the tungsten inert-gas welding of the IN718 superalloy, MET MAT T A, 32(7), 2001, pp. 1713-1725

Authors: Incze, LS Hebert, D Wolff, N Oakey, N Dye, D
Citation: Ls. Incze et al., Changes in copepod distributions associated with increased turbulence fromwind stress, MAR ECOL-PR, 213, 2001, pp. 229-240

Authors: Hunziker, O Dye, D Reed, RC
Citation: O. Hunziker et al., On the formation of a centreline grain boundary during fusion welding, ACT MATER, 48(17), 2000, pp. 4191-4201

Authors: Leonard, H Fyfe, S Dye, D Hockey, A Christodoulou, J
Citation: H. Leonard et al., Family data in Rett syndrome: Association with other genetic disorders, J PAEDIAT C, 36(4), 2000, pp. 336-339

Authors: Chandler, D Angelicheva, D Heather, L Gooding, R Gresham, D Yanakiev, P de Jonge, R Baas, F Dye, D Karagyozov, L Savov, A Blechschmidt, K Keats, B Thomas, PK King, RHM Starr, A Nikolova, A Colomer, J Ishpekova, B Tournev, I Urtizberea, JA Merlini, L Butinar, D Chabrol, B Voit, T Baethmann, M Nedkova, V Corches, A Kalaydjieva, L
Citation: D. Chandler et al., Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries, NEUROMUSC D, 10(8), 2000, pp. 584-591

Authors: Dye, D Roberts, SM Withers, PJ Reed, RC
Citation: D. Dye et al., The determination of the residual strains and stresses in a tungsten inertgas welded sheet of IN718 superalloy using neutron diffraction, J STRAIN A, 35(4), 2000, pp. 247-259

Authors: Leonard, H Fyfe, S Dye, D Leonard, S
Citation: H. Leonard et al., Using genetic epidemiology to study Rett syndrome: the design of a case-control study, PAED PERIN, 14(1), 2000, pp. 85-95

Authors: Angelicheva, D Turnev, I Dye, D Chandler, D Thomas, PK Kalaydjieva, L
Citation: D. Angelicheva et al., Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter, EUR J HUM G, 7(5), 1999, pp. 560-566

Authors: Fyfe, S Leonard, H Dye, D Leonard, S
Citation: S. Fyfe et al., Patterns of pregnancy loss, perinatal mortality, and postneonatal childhood deaths in families of girls with Rett syndrome, J CHILD NEU, 14(7), 1999, pp. 440-445

Authors: Leonard, H Fyfe, S Dye, D Leonard, S
Citation: H. Leonard et al., Familial aggregation in Rett syndrome: What is the evidence for clusteringof other disorders in the families of affected girls?, AM J MED G, 82(3), 1999, pp. 228-234

Authors: Kalaydjieva, L Perez-Lezaun, A Angelicheva, D Onengut, S Dye, D Bosshard, NU Jordanova, A Savov, A Yanakiev, P Kremensky, I Radeva, B Hallmayer, J Markov, A Nedkova, V Tournev, I Aneva, L Gitzelmann, R
Citation: L. Kalaydjieva et al., A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies), AM J HU GEN, 65(5), 1999, pp. 1299-1307
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