APA (7th ed.) Citation

Pacault, M., Vincent, M., Besnard, T., Kannengiesser, C., Bénéteau, C., Barbarot, S., . . . Dufernez, F. (2018). New splicing pathogenic variant in EBP causing extreme familial variability of Conradi–Hünermann–Happle Syndrome. European Journal of Human Genetics, 26(12), 1784. https://doi.org/10.1038/s41431-018-0217-0

Chicago Style (17th ed.) Citation

Pacault, Mathilde, et al. "New Splicing Pathogenic Variant in EBP Causing Extreme Familial Variability of Conradi–Hünermann–Happle Syndrome." European Journal of Human Genetics 26, no. 12 (2018): 1784. https://doi.org/10.1038/s41431-018-0217-0.

MLA (9th ed.) Citation

Pacault, Mathilde, et al. "New Splicing Pathogenic Variant in EBP Causing Extreme Familial Variability of Conradi–Hünermann–Happle Syndrome." European Journal of Human Genetics, vol. 26, no. 12, 2018, p. 1784, https://doi.org/10.1038/s41431-018-0217-0.