APA (7th ed.) Citation

S, F., L, V., A, V., M, A., A, R., C, C., . . . G, P. (2025). Combined biochemical profiling and DNA sequencing in the expanded newborn screening for inherited metabolic diseases: The experience in an Italian reference center. Orphanet journal of rare diseases, 20(1), 38. https://doi.org/10.1186/s13023-025-03546-1

Chicago Style (17th ed.) Citation

S, Fecarotta, et al. "Combined Biochemical Profiling and DNA Sequencing in the Expanded Newborn Screening for Inherited Metabolic Diseases: The Experience in an Italian Reference Center." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 38. https://doi.org/10.1186/s13023-025-03546-1.

MLA (9th ed.) Citation

S, Fecarotta, et al. "Combined Biochemical Profiling and DNA Sequencing in the Expanded Newborn Screening for Inherited Metabolic Diseases: The Experience in an Italian Reference Center." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 38, https://doi.org/10.1186/s13023-025-03546-1.