Search results

  • 2021

    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.

    Research output: Contribution to journalArticleAcademicpeer-review

    Open Access