APA (7th ed.) Citation

Lal, P., Lee, J., Adams, H., Yao, L., Fuhlbrück1, F., Yaung, S., . . . Rosenthal1, A. (2018). Abstract 2960: Concordance of genomic single-nucleotide variations (SNV) by next-generation sequencing (NGS) in paired tumor tissue and plasma in colorectal cancer (CRC). Cancer research (Chicago, Ill.), 78(13_Supplement), 2960. https://doi.org/10.1158/1538-7445.AM2018-2960

Chicago Style (17th ed.) Citation

Lal, Preeti, et al. "Abstract 2960: Concordance of Genomic Single-nucleotide Variations (SNV) by Next-generation Sequencing (NGS) in Paired Tumor Tissue and Plasma in Colorectal Cancer (CRC)." Cancer Research (Chicago, Ill.) 78, no. 13_Supplement (2018): 2960. https://doi.org/10.1158/1538-7445.AM2018-2960.

MLA (9th ed.) Citation

Lal, Preeti, et al. "Abstract 2960: Concordance of Genomic Single-nucleotide Variations (SNV) by Next-generation Sequencing (NGS) in Paired Tumor Tissue and Plasma in Colorectal Cancer (CRC)." Cancer Research (Chicago, Ill.), vol. 78, no. 13_Supplement, 2018, p. 2960, https://doi.org/10.1158/1538-7445.AM2018-2960.