Detection of low temperature oxidation of coal on a microscopic scale using secondary ion mass spectrometry von Martin, R.R., McIntyre, N.S., Winder, C.G., Sanders, D.C., Johnston, D.D., McPhee, J.A.

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G.P.312 von Bharucha-Goebel, D.X, Neil, E, Donkervoort, S, Moore, S, Winder, T, Dastgir, J, Iannaccone, S, Bönnemann, C.G

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G.P.152 von Leach, M.E, Donkervoort, S, Simpson, K, Tesi-Rocha, A.C, Avery, R, Dastgir, J, Reyes, C, Hu, Y, Winder, T.L, Bönnemann, C.G

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G.P.312: Intrafamilial variability in GMPPB associated alpha-dystroglycanopathy and broadening of the clinical phenotype von Bharucha-Goebel, D.X., Neil, E., Donkervoort, S., Moore, S., Winder, T., Dastgir, J., Iannaccone, S., Bönnemann, C.G.

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G.P.152: Novel recessive mutations in MYH2 presenting with congenital facial weakness, ophthalmoparesis, severe progressive scoliosis, and mild muscle weakness von Leach, M.E., Donkervoort, S., Simpson, K., Tesi-Rocha, A.C., Avery, R., Dastgir, J., Reyes, C., Hu, Y., Winder, T.L., Bönnemann, C.G.

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P1.11 Large genomic deletions as a novel type of mutation in Ullrich CMD von Foley, A.R, Hu, Y, Zou, Y, Yang, M, Medne, L, Leach, M, Conlin, L, Spinner, N, Shaikh, T, Neumeyer, A.M, Bliss, L, Winder, T, Bönnemann, C.G

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Hepatic and pulmonary enzyme activities in horses von Lakritz, J, Winder, B.S, Noorouz-Zadeh, J, Huang, T.L, Buckpitt, A.R, Hammock, B.D, Plopper, C.G

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