APA (7th ed.) Citation

Yan, L., Cao, J., Zhang, Y., Liu, Y., Zou, J., Lou, B., . . . Li, H. (2023). Prenatal diagnosis to identify compound heterozygous variants in PKDCC that causes rhizomelic limb shortening with dysmorphic features in a fetus from China. BMC Medical Genomics, 16(1), 1. https://doi.org/10.1186/s12920-023-01631-7

Chicago Style (17th ed.) Citation

Yan, Lulu, Juan Cao, Yuxin Zhang, Yingwen Liu, Jinghui Zou, Biying Lou, Danyan Zhuang, and Haibo Li. "Prenatal Diagnosis to Identify Compound Heterozygous Variants in PKDCC That Causes Rhizomelic Limb Shortening with Dysmorphic Features in a Fetus from China." BMC Medical Genomics 16, no. 1 (2023): 1. https://doi.org/10.1186/s12920-023-01631-7.

MLA (9th ed.) Citation

Yan, Lulu, et al. "Prenatal Diagnosis to Identify Compound Heterozygous Variants in PKDCC That Causes Rhizomelic Limb Shortening with Dysmorphic Features in a Fetus from China." BMC Medical Genomics, vol. 16, no. 1, 2023, p. 1, https://doi.org/10.1186/s12920-023-01631-7.