APA (7th ed.) Citation

J, Z., N, H., J, W., & C, C. (2026). Molecular diagnosis of rare biallelic CDC45 gene variants causing Meier-Gorlin syndrome-7 using whole exome sequencing. Human genomics, 20(1), . https://doi.org/10.1186/s40246-026-00922-1

Chicago Style (17th ed.) Citation

J, Zhuang, Huang N, Wang J, and Chen C. "Molecular Diagnosis of Rare Biallelic CDC45 Gene Variants Causing Meier-Gorlin Syndrome-7 Using Whole Exome Sequencing." Human Genomics 20, no. 1 (2026). https://doi.org/10.1186/s40246-026-00922-1.

MLA (9th ed.) Citation

J, Zhuang, et al. "Molecular Diagnosis of Rare Biallelic CDC45 Gene Variants Causing Meier-Gorlin Syndrome-7 Using Whole Exome Sequencing." Human Genomics, vol. 20, no. 1, 2026, https://doi.org/10.1186/s40246-026-00922-1.