APA (7th ed.) Citation

AA, B., LE, W., LC, P., & YH, W. (2009). Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites. BMC genomics, 10, 59. https://doi.org/10.1186/1471-2164-10-59

Chicago Style (17th ed.) Citation

AA, Burrow, Williams LE, Pierce LC, and Wang YH. "Over Half of Breakpoints in Gene Pairs Involved in Cancer-specific Recurrent Translocations Are Mapped to Human Chromosomal Fragile Sites." BMC Genomics 10 (2009): 59. https://doi.org/10.1186/1471-2164-10-59.

MLA (9th ed.) Citation

AA, Burrow, 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. 59, https://doi.org/10.1186/1471-2164-10-59.