Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1.

MLA

Lin, Tingting, et al. “Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1.” Frontiers in Genetics, vol. 13, Mar. 2022, pp. 1–9. EBSCOhost, https://doi.org/10.3389/fgene.2022.843931.

APA

Lin, T., Ma, Y., Zhou, D., Sun, L., Chen, K., Xiang, Y., Tong, K., Jia, C., Jiang, K., Liu, D., & Huang, G. (2022). Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1. Frontiers in Genetics, 13, 1–9. https://doi.org/10.3389/fgene.2022.843931

Chicago

Lin, Tingting, Yongyi Ma, Danni Zhou, Liwei Sun, Ke Chen, Yezhou Xiang, Keya Tong, et al. 2022. “Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1.” Frontiers in Genetics 13 (March): 1–9. doi:10.3389/fgene.2022.843931.