Search results
Results: 77,139
Number of items: 77,139
-
Petrij, F., Dauwerse, H. G., Blough, R. I., Giles, R. H., van der Smagt, J. J., Wallerstein, R., Maaswinkel-Mooy, P. D., van Karnebeek, C. D., van Ommen, G.-JB., van Haeringen, A., Rubinstein, J. H., Saal, H. M., Hennekam, R. C. M., Peters, D. J. M., & Breuning, M. H. (2000). Diagnostic analysis of th Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations. Journal of Medical Genetics, 37, 168-176. https://doi.org/10.1136/jmg.37.3.168 -
Nücker, N., Merz, M., Kuntscher, C. A., Gerhold, S., Schuppler, S., Neudert, R., Golden, M. S., Fink, J., & Schild, D. (2000). Hole distribution for (Sr,Ca,Y,La)14Cu24O41 ladder compounds studied by x-ray absorption spectroscopy. Physical Review B, 62, 14384-14392. https://doi.org/10.1103/PhysRevB.62.14384 -
Tuynman, A., Lutje Spelberg, J., Kooter, I. M., Schoemaker, H. E., & Wever, R. (2000). Enantioselective Epoxidation and Carbon–Carbon Bond Cleavage Catalyzed by Coprinus cinereus Peroxidase and Myeloperoxidase. The Journal of Biological Chemistry, 275(5), 3025-3030. https://doi.org/10.1074/jbc.275.5.3025 -
Crow, Y. J., Jackson, A. P., Roberts, E., van Beusekom, E., Barth, P. G., Corry, P., Ferrie, C. D., Hamel, B. C. J., Jayatunga, R., Karbani, G., Kálmánchey, R., Kelemen, A., King, M., Kumar, R., Livingstone, J., Massey, R., McWilliam, R., Meager, A., Rittey, C., ... Woods, C. G. (2000). Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21. American Journal of Human Genetics, 67, 213-221.
Page 7108 of 7714