Published in Cancer Weekly, December 30th, 2003
Investigators say the results of the study of 11,085 women should facilitate earlier treatment, while allowing others to avoid unnecessary, invasive follow-up procedures.
The study was published in the December 6, 2003, issue of The Lancet
The research used Digene Corp.'s (DIGE) DNAwithPap Test, which is the only Food and Drug Administration (FDA)-approved test that detects the presence of the human papillomavirus - the primary cause...
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Source: Cancer Weekly (2003-12-30)
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