Dias, C., Pfundt, R., Kleefstra, T., Shuurs‐Hoeijmakers, J., Boon, E. M. J., van Hagen, J. M., Zwijnenburg, P., Weiss, M. M., Keren, B., Mignot, C., Isapof, A., Weiss, K., Hershkovitz, T., Iascone, M., Maitz, S., Feichtinger, R. G., Kotzot, D., Mayr, J. A., Ben‐Omran, T., Mahmoud, L., Pais, L. S., Walsh, C. A., Shashi, V., Sullivan, J. A., Stong, N., Lecoquierre, F., Guerrot, A., Charollais, A., & Rodan, L. H. (2021). de novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder. American journal of medical genetics, 185(8), 2384–2390. http://access.bl.uk/ark:/81055/vdc_100134857455.0x000018