APA (7th ed.) Citation

Xi, H., Xie, W., Chen, J., Tang, W., Deng, X., Li, H., . . . Wang, H. (2021). Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center. Molecular genetics & genomic medicine, 9(7), e1711-n/a. https://doi.org/10.1002/mgg3.1711

Chicago Style (17th ed.) Citation

Xi, Hui, et al. "Implementation of Fragile X Syndrome Carrier Screening During Prenatal Diagnosis: A Pilot Study at a Single Center." Molecular Genetics & Genomic Medicine 9, no. 7 (2021): e1711-n/a. https://doi.org/10.1002/mgg3.1711.

MLA (9th ed.) Citation

Xi, Hui, et al. "Implementation of Fragile X Syndrome Carrier Screening During Prenatal Diagnosis: A Pilot Study at a Single Center." Molecular Genetics & Genomic Medicine, vol. 9, no. 7, 2021, pp. e1711-n/a, https://doi.org/10.1002/mgg3.1711.