APA (7th ed.) Citation

S, N., I, K., A, S., R, A. J., T, B., J, D., . . . B, P. (2022). Prenatal phenotype of PNKP-related primary microcephaly associated with variants affecting both the FHA and phosphatase domain. European journal of human genetics : EJHG, 30(1), 101. https://doi.org/10.1038/s41431-021-00982-y

Chicago Style (17th ed.) Citation

S, Neuser, et al. "Prenatal Phenotype of PNKP-related Primary Microcephaly Associated with Variants Affecting Both the FHA and Phosphatase Domain." European Journal of Human Genetics : EJHG 30, no. 1 (2022): 101. https://doi.org/10.1038/s41431-021-00982-y.

MLA (9th ed.) Citation

S, Neuser, et al. "Prenatal Phenotype of PNKP-related Primary Microcephaly Associated with Variants Affecting Both the FHA and Phosphatase Domain." European Journal of Human Genetics : EJHG, vol. 30, no. 1, 2022, p. 101, https://doi.org/10.1038/s41431-021-00982-y.