APA (7th ed.) Citation

Shi, X., Tang, H., Lu, J., Yang, X., Ding, H., & Wu, J. (2021). Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing. Annals of medicine (Helsinki), 53(1), 1286-1292. https://doi.org/10.1080/07853890.2021.1962966

Chicago Style (17th ed.) Citation

Shi, Xiaomei, Hui Tang, Jian Lu, Xiue Yang, Hongke Ding, and Jing Wu. "Prenatal Genetic Diagnosis of Omphalocele by Karyotyping, Chromosomal Microarray Analysis and Exome Sequencing." Annals of Medicine (Helsinki) 53, no. 1 (2021): 1286-1292. https://doi.org/10.1080/07853890.2021.1962966.

MLA (9th ed.) Citation

Shi, Xiaomei, et al. "Prenatal Genetic Diagnosis of Omphalocele by Karyotyping, Chromosomal Microarray Analysis and Exome Sequencing." Annals of Medicine (Helsinki), vol. 53, no. 1, 2021, pp. 1286-1292, https://doi.org/10.1080/07853890.2021.1962966.