Diagnostic utility of transcriptome sequencing for rare Mendelian diseases.

MLA

Lee, Hane, et al. “Diagnostic Utility of Transcriptome Sequencing for Rare Mendelian Diseases.” Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 22, no. 3, Mar. 2020, pp. 490–99. EBSCOhost, https://doi.org/10.1038/s41436-019-0672-1.

APA

Lee, H., Huang, A. Y., Wang, L.-K., Yoon, A. J., Renteria, G., Eskin, A., Signer, R. H., Dorrani, N., Nieves-Rodriguez, S., Wan, J., Douine, E. D., Woods, J. D., Dell’Angelica, E. C., Fogel, B. L., Martin, M. G., Butte, M. J., Parker, N. H., Wang, R. T., Shieh, P. B., … Nelson, S. F. (2020). Diagnostic utility of transcriptome sequencing for rare Mendelian diseases. Genetics in Medicine : Official Journal of the American College of Medical Genetics, 22(3), 490–499. https://doi.org/10.1038/s41436-019-0672-1

Chicago

Lee, Hane, Alden Y Huang, Lee-Kai Wang, Amanda J Yoon, Genecee Renteria, Ascia Eskin, Rebecca H Signer, et al. 2020. “Diagnostic Utility of Transcriptome Sequencing for Rare Mendelian Diseases.” Genetics in Medicine : Official Journal of the American College of Medical Genetics 22 (3): 490–99. doi:10.1038/s41436-019-0672-1.