APA (7th ed.) Citation

Li, L., Zhang, J., Li, Q., Qiao, L., Li, P., Cui, Y., . . . Yang, H. (2022). Mutational analysis of compound heterozygous mutation p.Q6X/p.H232R in SRD5A2 causing 46,XY disorder of sex development. Italian journal of pediatrics, 48(1), 47-13. https://doi.org/10.1186/s13052-022-01243-4

Chicago Style (17th ed.) Citation

Li, Liwei, et al. "Mutational Analysis of Compound Heterozygous Mutation P.Q6X/p.H232R in SRD5A2 Causing 46,XY Disorder of Sex Development." Italian Journal of Pediatrics 48, no. 1 (2022): 47-13. https://doi.org/10.1186/s13052-022-01243-4.

MLA (9th ed.) Citation

Li, Liwei, et al. "Mutational Analysis of Compound Heterozygous Mutation P.Q6X/p.H232R in SRD5A2 Causing 46,XY Disorder of Sex Development." Italian Journal of Pediatrics, vol. 48, no. 1, 2022, pp. 47-13, https://doi.org/10.1186/s13052-022-01243-4.