Saier, C., Sansen, S., Berghout, J., Freyler, K., Einhorn, M., Einhorn, Y., . . . Kirschner, J. (2025). TREAT: Systematic and inclusive selection process of genes for genomic newborn screening as part of the Screen4Care project. Orphanet Journal of Rare Diseases, 20(1), . https://doi.org/10.1186/s13023-025-03692-6
Παραπομπή σε μορφή Chicago (17η εκδ.)Saier, Christina, et al. "TREAT: Systematic and Inclusive Selection Process of Genes for Genomic Newborn Screening as Part of the Screen4Care Project." Orphanet Journal of Rare Diseases 20, no. 1 (2025). https://doi.org/10.1186/s13023-025-03692-6.
Παραπομπή σε μορφή MLA (9th εκδ.)Saier, Christina, et al. "TREAT: Systematic and Inclusive Selection Process of Genes for Genomic Newborn Screening as Part of the Screen4Care Project." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, https://doi.org/10.1186/s13023-025-03692-6.