APA (7th ed.) Citation

X, T., Z, W., S, Y., M, C., Y, Z., F, Z., . . . L, W. (2022). Maternal Xp22.31 copy-number variations detected in non-invasive prenatal screening effectively guide the prenatal diagnosis of X-linked ichthyosis. Frontiers in genetics, 13, 934952. https://doi.org/10.3389/fgene.2022.934952

Chicago Style (17th ed.) Citation

X, Tang, Wang Z, Yang S, Chen M, Zhang Y, Zhang F, Tan J, Yin T, and Wang L. "Maternal Xp22.31 Copy-number Variations Detected in Non-invasive Prenatal Screening Effectively Guide the Prenatal Diagnosis of X-linked Ichthyosis." Frontiers in Genetics 13 (2022): 934952. https://doi.org/10.3389/fgene.2022.934952.

MLA (9th ed.) Citation

X, Tang, et al. "Maternal Xp22.31 Copy-number Variations Detected in Non-invasive Prenatal Screening Effectively Guide the Prenatal Diagnosis of X-linked Ichthyosis." Frontiers in Genetics, vol. 13, 2022, p. 934952, https://doi.org/10.3389/fgene.2022.934952.