User:JMILES19/Wiedemann–Steiner syndrome/Bibliography

Bibliography for Wiedemann–Steiner syndrome

Koenig, R., Meinecke, P., Kuechler, A., Schäfer, D., & Müller, D. (2010). Wiedemann-Steiner syndrome: Three further cases. American Journal of Medical Genetics Part A, 152A(9), 2372–2375. https://doi.org/10.1002/ajmg.a.33587

Sun, Y., Hu, G., Liu, H., Zhang, X., Huang, Z., Yan, H., Wang, L., Fan, Y., Gu, X., & Yu, Y. (2016). Further delineation of the phenotype of truncating KMT2A mutations: The extended Wiedemann-Steiner syndrome. American Journal of Medical Genetics Part A, 173(2), 510–514. https://doi.org/10.1002/ajmg.a.38025

Grangeia, A., Leão, M., & Moura, C. P. (2019). Wiedemann‐Steiner syndrome in two patients from Portugal. American Journal of Medical Genetics Part A, 182(1), 25–28. https://doi.org/10.1002/ajmg.a.61407

Baer, S., Afenjar, A., Smol, T., Piton, A., Gérard, B., Alembik, Y., Bienvenu, T., Boursier, G., Boute, O., Colson, C., Cordier, M. P., Cormier-Daire, V., Delobel, B., Doco-Fenzy, M., Duban-Bedu, B., Fradin, M., Geneviève, D., Goldenberg, A., Grelet, M.,. . . Morin, G. (2018). Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases. Clinical Genetics, 94(1), 141–152. https://doi.org/10.1111/cge.13254

Aggarwal, A., Rodriguez-Buritica, D. F., & Northrup, H. (2017). Wiedemann-Steiner syndrome: Novel pathogenic variant and review of literature. European Journal of Medical Genetics, 60(6), 285–288. https://doi.org/10.1016/j.ejmg.2017.03.006