APA (7th ed.) Citation

A, S., M, D., K, G., T, B., H, K., TC, H., . . . M, W. (2024). Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings. Nature genetics, 56(8), 1644. https://doi.org/10.1038/s41588-024-01836-1

Chicago Style (17th ed.) Citation

A, Schmidt, et al. "Next-generation Phenotyping Integrated in a National Framework for Patients with Ultrarare Disorders Improves Genetic Diagnostics and Yields New Molecular Findings." Nature Genetics 56, no. 8 (2024): 1644. https://doi.org/10.1038/s41588-024-01836-1.

MLA (9th ed.) Citation

A, Schmidt, et al. "Next-generation Phenotyping Integrated in a National Framework for Patients with Ultrarare Disorders Improves Genetic Diagnostics and Yields New Molecular Findings." Nature Genetics, vol. 56, no. 8, 2024, p. 1644, https://doi.org/10.1038/s41588-024-01836-1.