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Joris Veltman

20152015

Research output per year

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Research Output

De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum

Kuechler, A., Willemsen, M. H., Albrecht, B., Bacino, C. A., Bartholomew, D. W., van Bokhoven, H., van den Boogaard, M. J. H., Bramswig, N., Büttner, C., Cremer, K., Czeschik, J. C., Engels, H., van Gassen, K., Graf, E., van Haelst, M., He, W., Hogue, J. S., Kempers, M., Koolen, D., Monroe, G. & 18 others, de Munnik, S., Pastore, M., Reis, A., Reuter, M. S., Tegay, D. H., Veltman, J., Visser, G., van Hasselt, P., Smeets, E. E. J., Vissers, L., Wieland, T., Wissink, W., Yntema, H., Zink, A. M., Strom, T. M., Lüdecke, H-J., Kleefstra, T. & Wieczorek, D., Jan 2015, In : Human Genetics. 134, 1, p. 97-109 13 p.

Research output: Contribution to journalArticleAcademicpeer-review