APA (7th ed.) Citation

AM, H., R, V., EA, V., DA, C., K, W., E, T., . . . BA, R. (2022). Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling. Genetics in medicine : official journal of the American College of Medical Genetics, 24(10), 2065. https://doi.org/10.1016/j.gim.2022.07.005

Chicago Style (17th ed.) Citation

AM, Holtz, et al. "Heterozygous Variants in MYH10 Associated with Neurodevelopmental Disorders and Congenital Anomalies with Evidence for Primary Cilia-dependent Defects in Hedgehog Signaling." Genetics in Medicine : Official Journal of the American College of Medical Genetics 24, no. 10 (2022): 2065. https://doi.org/10.1016/j.gim.2022.07.005.

MLA (9th ed.) Citation

AM, Holtz, et al. "Heterozygous Variants in MYH10 Associated with Neurodevelopmental Disorders and Congenital Anomalies with Evidence for Primary Cilia-dependent Defects in Hedgehog Signaling." Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 24, no. 10, 2022, p. 2065, https://doi.org/10.1016/j.gim.2022.07.005.