T, C., MQ, S., F, X., LL, H., LL, L., KC, Z., . . . LS, H. (2026). Combined biochemical and genetic analysis improves early diagnosis and prenatal assessment of multiple acyl-CoA dehydrogenase deficiency. World journal of pediatrics : WJP, 22(5), 596. https://doi.org/10.1007/s12519-026-01032-7
Chicago Style (17th ed.) CitationT, Chen, et al. "Combined Biochemical and Genetic Analysis Improves Early Diagnosis and Prenatal Assessment of Multiple Acyl-CoA Dehydrogenase Deficiency." World Journal of Pediatrics : WJP 22, no. 5 (2026): 596. https://doi.org/10.1007/s12519-026-01032-7.
MLA (9th ed.) CitationT, Chen, et al. "Combined Biochemical and Genetic Analysis Improves Early Diagnosis and Prenatal Assessment of Multiple Acyl-CoA Dehydrogenase Deficiency." World Journal of Pediatrics : WJP, vol. 22, no. 5, 2026, p. 596, https://doi.org/10.1007/s12519-026-01032-7.