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  • Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome

    Weerts, M. J. A., Lanko, K., Guzman-Vega, F. J., Jackson, A., Ramakrishnan, R., Cardona-Londono, K. J., Pena-Guerra, K. A., van Bever, Y., van Paassen, B. W., Kievit, A., van Slegtenhorst, M., Allen, N. M., Kehoe, C. M., Robinson, H. K., Pang, L., Banu, S. H., Zaman, M., Efthymiou, S., Houlden, H., Jarvela, I., & 32 othersLauronen, L., Maatta, T., Schrauwen, I., Leal, S. M., Ruivenkamp, C. A. L., Barge-Schaapveld, D. Q. C. M., Peeters-Scholte, C. M. P. C. D., Galehdari, H., Mazaheri, N., Sisodiya, S. M., Harrison, V., Sun, A., Thies, J., Pedroza, L. A., Lara-Taranchenko, Y., Chinn, I. K., Lupski, J. R., Garza-Flores, A., McGlothlin, J., Yang, L., Huang, S., Wang, X., Jewett, T., Rosso, G., Lin, X., Mohammed, S., Merritt, J. L., Mirzaa, G. M., Willemsen, M., Koning, S., Genomics England Research Consortium & Barakat, T. S., Nov 2021, In: Genetics in Medicine. 23, 11, p. 2122-2137 16 p.

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    Open Access
    6 Citations (Web of Science)