Cita APA (7a ed.)
Hegde, M., Santani, A., Mao, R., Ferreira-Gonzalez, A., Weck, K. E., & Voelkerding, K. V. (2017). Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease. Archives of Pathology & Laboratory Medicine, 141(6), 798-806.
Cita Chicago Style (17a ed.)
Hegde, Madhuri, Avni Santani, Rong Mao, Andrea Ferreira-Gonzalez, Karen E. Weck, y Karl V. Voelkerding. "Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease." Archives of Pathology & Laboratory Medicine 141, no. 6 (2017): 798-806.
Cita MLA (9a ed.)
Hegde, Madhuri, et al. "Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease." Archives of Pathology & Laboratory Medicine, vol. 141, no. 6, 2017, pp. 798-806.
Precaución: Estas citas no son 100% exactas.