APA (7th ed.) Citation

E, W., AØ, R., L, B., JB, C., K, G., II, I., . . . AM, J. (2026). Case Series: Clinical Significance of Heterozygous Pathogenic RTEL1 Variants Identified via Routine Clinical Genetic Diagnostics. American journal of medical genetics. Part A, 200(4), 959. https://doi.org/10.1002/ajmga.70015

Chicago Style (17th ed.) Citation

E, Wedge, et al. "Case Series: Clinical Significance of Heterozygous Pathogenic RTEL1 Variants Identified via Routine Clinical Genetic Diagnostics." American Journal of Medical Genetics. Part A 200, no. 4 (2026): 959. https://doi.org/10.1002/ajmga.70015.

MLA (9th ed.) Citation

E, Wedge, et al. "Case Series: Clinical Significance of Heterozygous Pathogenic RTEL1 Variants Identified via Routine Clinical Genetic Diagnostics." American Journal of Medical Genetics. Part A, vol. 200, no. 4, 2026, p. 959, https://doi.org/10.1002/ajmga.70015.