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Author Title Type [ Year(Asc)]
Filters: Author is Grados, Marco  [Clear All Filters]
2018
A. D. Kline, Moss, J. F., Selicorni, A., Bisgaard, A. - M., Deardorff, M. A., Gillett, P. M., Ishman, S. L., Kerr, L. M., Levin, A. V., Mulder, P. A., Ramos, F. J., Wierzba, J., Ajmone, P. Francesca, Axtell, D., Blagowidow, N., Cereda, A., Costantino, A., Cormier-Daire, V., FitzPatrick, D., Grados, M., Groves, L., Guthrie, W., Huisman, S., Kaiser, F. J., Koekkoek, G., Levis, M., Mariani, M., McCleery, J. P., Menke, L. A., Metrena, A., O'Connor, J., Oliver, C., Pie, J., Piening, S., Potter, C. J., Quaglio, A. L., Redeker, E., Richman, D., Rigamonti, C., Shi, A., Tümer, Z., Van Balkom, I. D. C., and Hennekam, R. C., “Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement.”, Nat Rev Genet, vol. 19, no. 10, pp. 649-666, 2018.
2017
A. D. Kline, Krantz, I. D., Deardorff, M. A., Shirahige, K., Dorsett, D., Gerton, J. L., Wu, M., Mehta, D., Mills, J. A., Carrico, C. S., Noon, S., Herrera, P. S., Horsfield, J. A., Bettale, C., Morgan, J., Huisman, S. A., Moss, J., McCleery, J., Grados, M., Hansen, B. D., Srivastava, S., Taylor-Snell, E., Kerr, L. M., Katz, O., Calof, A. L., Musio, A., Egense, A., and Haaland, R. E., “Cornelia de Lange syndrome and molecular implications of the cohesin complex: Abstracts from the 7th biennial scientific and educational symposium 2016.”, Am J Med Genet A, vol. 173, no. 5, pp. 1172-1185, 2017.