Transcript capture and ultradeep long-read RNA sequencing (CAPLRseq) to diagnose HNPCC/Lynch syndrome.

MLA

Schwenk, Vincent, et al. “Transcript Capture and Ultradeep Long-Read RNA Sequencing (CAPLRseq) to Diagnose HNPCC/Lynch Syndrome.” Journal of Medical Genetics, vol. 60, no. 8, Aug. 2023, pp. 747–59. EBSCOhost, https://doi.org/10.1136/jmg-2022-108931.

APA

Schwenk, V., Leal Silva, R. M., Scharf, F., Knaust, K., Wendlandt, M., Häusser, T., Pickl, J. M. A., Steinke-Lange, V., Laner, A., Morak, M., Holinski-Feder, E., & Wolf, D. A. (2023). Transcript capture and ultradeep long-read RNA sequencing (CAPLRseq) to diagnose HNPCC/Lynch syndrome. Journal of Medical Genetics, 60(8), 747–759. https://doi.org/10.1136/jmg-2022-108931

Chicago

Schwenk, Vincent, Rafaela Magalhaes Leal Silva, Florentine Scharf, Katharina Knaust, Martin Wendlandt, Tanja Häusser, Julia M A Pickl, et al. 2023. “Transcript Capture and Ultradeep Long-Read RNA Sequencing (CAPLRseq) to Diagnose HNPCC/Lynch Syndrome.” Journal of Medical Genetics 60 (8): 747–59. doi:10.1136/jmg-2022-108931.