Elbracht, M., Krause, J., Mattern, L., Güzel, N., Lischka, A., Suh, D. S. J., . . . Kurth, I. (2026). Exome and Genome Sequencing for the Diagnosis of Rare. Deutsches Ärzteblatt International, 123(7), 1. https://doi.org/10.3238/arztebl.m2026.0030
Chicago Style (17th ed.) CitationElbracht, M., et al. "Exome and Genome Sequencing for the Diagnosis of Rare." Deutsches Ärzteblatt International 123, no. 7 (2026): 1. https://doi.org/10.3238/arztebl.m2026.0030.
MLA (9th ed.) CitationElbracht, M., et al. "Exome and Genome Sequencing for the Diagnosis of Rare." Deutsches Ärzteblatt International, vol. 123, no. 7, 2026, p. 1, https://doi.org/10.3238/arztebl.m2026.0030.
Warning: These citations may not always be 100% accurate.