Schmidt, A., Danyel, M., Grundmann-Hauser, K., Brunet, T., Klinkhammer, H., Hsieh, T., . . . Bettendorf, M. (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), . https://doi.org/10.1038/s41588-024-01836-1
Chicago-Zitierstil (17. Ausg.)Schmidt, Axel, 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). https://doi.org/10.1038/s41588-024-01836-1.
MLA-Zitierstil (9. Ausg.)Schmidt, Axel, 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, https://doi.org/10.1038/s41588-024-01836-1.