APA (7th ed.) Citation

Burrow, A. A., Williams, L. E., Pierce, L. C. T., & Wang, Y. (2009). Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites. BMC Genomics, 10, 1. https://doi.org/10.1186/1471-2164-10-59

Chicago Style (17th ed.) Citation

Burrow, Allison A., Laura E. Williams, Levi C. T. Pierce, and Yuh-Hwa Wang. "Over Half of Breakpoints in Gene Pairs Involved in Cancer-specific Recurrent Translocations Are Mapped to Human Chromosomal Fragile Sites." BMC Genomics 10 (2009): 1. https://doi.org/10.1186/1471-2164-10-59.

MLA (9th ed.) Citation

Burrow, Allison A., et al. "Over Half of Breakpoints in Gene Pairs Involved in Cancer-specific Recurrent Translocations Are Mapped to Human Chromosomal Fragile Sites." BMC Genomics, vol. 10, 2009, p. 1, https://doi.org/10.1186/1471-2164-10-59.