APA (7th ed.) Citation

D, B., E, B., S, L., TN, E., M, O., I, O., . . . LC, B. (2024). Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Human genetics, 143(3), 279. https://doi.org/10.1007/s00439-024-02657-2

Chicago Style (17th ed.) Citation

D, Brooks, et al. "Heterozygous MAP3K20 Variants Cause Ectodermal Dysplasia, Craniosynostosis, Sensorineural Hearing Loss, and Limb Anomalies." Human Genetics 143, no. 3 (2024): 279. https://doi.org/10.1007/s00439-024-02657-2.

MLA (9th ed.) Citation

D, Brooks, et al. "Heterozygous MAP3K20 Variants Cause Ectodermal Dysplasia, Craniosynostosis, Sensorineural Hearing Loss, and Limb Anomalies." Human Genetics, vol. 143, no. 3, 2024, p. 279, https://doi.org/10.1007/s00439-024-02657-2.