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Among women with HNPCC, this study will assess:
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Women who are at risk for HNPCC will be recruited to participate in this pilot study.
Women will be invited to participate in the study either through a mailed invitation or during a visit to M.D. Anderson for clinical services or for research purposes.
Women who wish to participate in the study will complete an informed consent, and will subsequently schedule an appointment with a research coordinator to complete the study questionnaire by telephone.
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93 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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