APA (7th ed.) Citation

JM, K., HW, C., DM, S., OH, K., J, K., H, L., . . . MH, P. (2025). Uncovering potential causal genes for undiagnosed congenital anomalies using an in-house pipeline for trio-based whole-genome sequencing. Human genomics, 19(1), 1. https://doi.org/10.1186/s40246-024-00709-2

Chicago Style (17th ed.) Citation

JM, Kim, et al. "Uncovering Potential Causal Genes for Undiagnosed Congenital Anomalies Using an In-house Pipeline for Trio-based Whole-genome Sequencing." Human Genomics 19, no. 1 (2025): 1. https://doi.org/10.1186/s40246-024-00709-2.

MLA (9th ed.) Citation

JM, Kim, et al. "Uncovering Potential Causal Genes for Undiagnosed Congenital Anomalies Using an In-house Pipeline for Trio-based Whole-genome Sequencing." Human Genomics, vol. 19, no. 1, 2025, p. 1, https://doi.org/10.1186/s40246-024-00709-2.