APA (7th ed.) Citation

Mazzonetto, P. C., Villela, D., da Costa, S. S., Krepischi, A. C. V., Milanezi, F., Migliavacca, M. P., . . . Rosenberg, C. (2024). Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting. Annals of Human Genetics, 88(2), 113. https://doi.org/10.1111/ahg.12532

Chicago Style (17th ed.) Citation

Mazzonetto, Patricia C., et al. "Low‐pass Whole Genome Sequencing Is a Reliable and Cost‐effective Approach for Copy Number Variant Analysis in the Clinical Setting." Annals of Human Genetics 88, no. 2 (2024): 113. https://doi.org/10.1111/ahg.12532.

MLA (9th ed.) Citation

Mazzonetto, Patricia C., et al. "Low‐pass Whole Genome Sequencing Is a Reliable and Cost‐effective Approach for Copy Number Variant Analysis in the Clinical Setting." Annals of Human Genetics, vol. 88, no. 2, 2024, p. 113, https://doi.org/10.1111/ahg.12532.