Hemati, P., Revah‐Politi, A., Bassan, H., Petrovski, S., Bilancia, C. G., Ramsey, K., Griffin, N. G., Bier, L., Cho, M. T., Rosello, M., Lynch, S. A., Colombo, S., Weber, A., Haug, M., Heinzen, E. L., Sands, T. T., Narayanan, V., Primiano, M., Aggarwal, V. S., Millan, F., Sattler‐Holtrop, S. G., Caro‐Llopis, A., Pillar, N., Baker, J., Freedman, R., Kroes, H. Y., Sacharow, S., Stong, N., Lapunzina, P., Schneider, M. C., Mendelsohn, N. J., Singleton, A., Loik Ramey, V., Wou, K., Kuzminsky, A., Monfort, S., Weisz Hubshman, M., Doyle, S., Iglesias, A., Martinez, F., Mckenzie, F., Orellana, C., van Gassen, K. L., Palomares, M., Bazak, L., Lee, A., Bircher, A., Basel‐Vanagaite, L., Hafström, M., Houge, G., , , , , Goldstein, D. B., & Anyane‐Yeboa, K. (2018). refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature. American journal of medical genetics, 176(11), 2259–2275. http://access.bl.uk/ark:/81055/vdc_100090656323.0x000019