Sprissler, R.; Perkins, B.; Johnstone, L.; Babiker, H.M.; Chalasani, P.; Lau, B.; Hammer, M.; Mahadevan, D.
Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations. Cancers 2020, 12, 1618.
https://doi.org/10.3390/cancers12061618
AMA Style
Sprissler R, Perkins B, Johnstone L, Babiker HM, Chalasani P, Lau B, Hammer M, Mahadevan D.
Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations. Cancers. 2020; 12(6):1618.
https://doi.org/10.3390/cancers12061618
Chicago/Turabian Style
Sprissler, Ryan, Bryce Perkins, Laurel Johnstone, Hani M. Babiker, Pavani Chalasani, Branden Lau, Michael Hammer, and Daruka Mahadevan.
2020. "Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations" Cancers 12, no. 6: 1618.
https://doi.org/10.3390/cancers12061618
APA Style
Sprissler, R., Perkins, B., Johnstone, L., Babiker, H. M., Chalasani, P., Lau, B., Hammer, M., & Mahadevan, D.
(2020). Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations. Cancers, 12(6), 1618.
https://doi.org/10.3390/cancers12061618