Biard, J.-M., Englebert, H., Destrée, A., Benoit, V., Carbonez, K., Ortegat, M., … Sznajer, Y. (2024). Diagnosis of Kabuki syndrome with unreported KMT2D pathogenic variant: contribution of prenatal facial dysmorphology analysis and whole exome sequencing – about a clinical report and review of the literature. European Gynecology & Obstetrics, 5(3). https://doi.org/10.53260/EGO.235037