APA (7th ed.) Citation

T, B., R, B., V, D., JS, H., D, C., S, A., . . . M, W. (2022). Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Human molecular genetics, 31(14), 2386. https://doi.org/10.1093/hmg/ddac034

Chicago Style (17th ed.) Citation

T, Brunet, et al. "Clonal Hematopoiesis as a Pitfall in Germline Variant Interpretation in the Context of Mendelian Disorders." Human Molecular Genetics 31, no. 14 (2022): 2386. https://doi.org/10.1093/hmg/ddac034.

MLA (9th ed.) Citation

T, Brunet, et al. "Clonal Hematopoiesis as a Pitfall in Germline Variant Interpretation in the Context of Mendelian Disorders." Human Molecular Genetics, vol. 31, no. 14, 2022, p. 2386, https://doi.org/10.1093/hmg/ddac034.