A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease.

MLA

Oliver, Gavin R., et al. “A Tailored Approach to Fusion Transcript Identification Increases Diagnosis of Rare Inherited Disease.” PloS One, vol. 14, no. 10, Oct. 2019, p. e0223337. EBSCOhost, https://doi.org/10.1371/journal.pone.0223337.

APA

Oliver, G. R., Tang, X., Schultz-Rogers, L. E., Vidal-Folch, N., Jenkinson, W. G., Schwab, T. L., Gaonkar, K., Cousin, M. A., Nair, A., Basu, S., Chanana, P., Oglesbee, D., & Klee, E. W. (2019). A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease. PloS One, 14(10), e0223337. https://doi.org/10.1371/journal.pone.0223337

Chicago

Oliver, Gavin R, Xiaojia Tang, Laura E Schultz-Rogers, Noemi Vidal-Folch, W Garrett Jenkinson, Tanya L Schwab, Krutika Gaonkar, et al. 2019. “A Tailored Approach to Fusion Transcript Identification Increases Diagnosis of Rare Inherited Disease.” PloS One 14 (10): e0223337. doi:10.1371/journal.pone.0223337.