APA (7th ed.) Citation

FN, T., NM, M., D, V., M, S., K, K., A, M., . . . C, S. (2023). Germline CNV Detection through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases. Genes, 14(7), . https://doi.org/10.3390/genes14071490

Chicago Style (17th ed.) Citation

FN, Tilemis, et al. "Germline CNV Detection Through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases." Genes 14, no. 7 (2023). https://doi.org/10.3390/genes14071490.

MLA (9th ed.) Citation

FN, Tilemis, et al. "Germline CNV Detection Through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases." Genes, vol. 14, no. 7, 2023, https://doi.org/10.3390/genes14071490.