Abstract
Synovial sarcoma shows a characteristic t(X;18) translocation but not the expected female predominance in incidence. We speculate that, among females, one X-chromosome is inactivated and that only the translocation to an active X-chromosome leads to development of synovial sarcoma. Population-based cancer registry data from the SEER program support this hypothesis. © 2002 Cancer Research UK.
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APA
Bu, X., Bernstein, L., & Brynes, R. K. (2002). Reduced risk of synovial sarcoma in females: X-chromosome inactivation? British Journal of Cancer, 87(1), 28–30. https://doi.org/10.1038/sj.bjc.6600362
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