Den Hoed, J., De Boer, E., Voisin, N., Guex, N., Snijders Blok, L., Chrast, J., The DDD study, Manwaring, L., Willing, M.,
Waheeb, A., Osmond, M., McWalter, K., Vitobello, A., Demurger, F., Lavillaureix, A., Odent, S., Mazel, B., Faivre, L., Thiffault,
I., Schwager, C., Amudhavalli, S. M., Rosenfeld, J. A., Radtke, K., Preiksaitiene, E., Ranza, E., Depienne, C., Kuechler,
A., Mohammed, S., Hamzavi Abedi, Y., Bonagura, V. R., Zuccarelli, B., Horist, B., Krishnamurthy, V., Kattentidt-Mouravieva,
A. A., Granger, L., Petersen, A., Jones, K. L., Sinnema, M., Stegmann, A. P. A., Newbury-Ecob, R., Kini, U., Newbury, D. F.,
Gilissen, C., Brunner, H., Kleefstra, T., Reymond, A., Vissers, L. E. L. M., & Fisher, S. E. (2020).
Mutation-specific pathophysiological mechanisms in a new SATB1 -associated neurodevelopmental disorder.
Talk presented at the 53rd European Human Genetics Conference (ESHG 2020). online. 2020-06-06 - 2020-06-09.
