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Ms. Hampel's research interests include screening all colorectal and endometrial cancer patients for Lynch syndrome, the American Founder Mutation (exon 1-6 deletion in MSH2) as a cause of Lynch syndrome, and the etiology of MSI-negative familial colorectal cancers. Ms. Hampel is currently serving a 5 year term on the American Board of Genetic Counselors (ABGC) and has been elected to serve as the President of ABGC for 2009.
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