Gross, A. M., Ajay, S. S., Rajan, V., Brown, C., Bluske, K., Burns, N. J., . . . Taft, R. J. (2018). Copy-number variants in clinical genome sequencing: Deployment and interpretation for rare and undiagnosed disease. Genet Med.
Chicago Style CitationGross, Andrew M., et al. "Copy-number Variants in Clinical Genome Sequencing: Deployment and Interpretation for Rare and Undiagnosed Disease." Genet Med 2018.
Cita MLAGross, Andrew M., et al. "Copy-number Variants in Clinical Genome Sequencing: Deployment and Interpretation for Rare and Undiagnosed Disease." Genet Med 2018.
Atenció: Aquestes cites poden no estar 100% correctes.