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Familial Cancer|May 24, 2007
The role of patient users in cancer genetics services in primary careMelanie Ripley, Deborah Sullivan, Jo Evans
Familial Cancer|September 1, 2006
Occurrence of both breast and ovarian cancer in a woman is a marker for the BRCA gene mutations: a population-based study from western SwedenZakaria Einbeigi, Annika Bergman, Jeanne M Meis-Kindblom, et al.
Familial Cancer|August 29, 2006
Awareness of gynecologic surveillance in women from hereditary non-polyposis colorectal cancer familiesKathleen Yang, Brian Allen, Peggy Conrad, et al.
Familial Cancer|October 14, 2006
The natural history of a combined defect in MSH6 and MUTYH in a HNPCC familyMarjo van Puijenbroek, Maartje Nielsen, Tjitske H C M Reinards, et al.
Familial Cancer|October 14, 2006
The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndromeSusan Stuckless, Patrick S Parfrey, Michael O Woods, et al.
Familial Cancer|June 1, 2006
Pharmacogenetics in the management of breast cancer -- prospects for individualised treatmentFiona H Blackhall, Sacha Howell, Bill Newman
Familial Cancer|June 1, 2006
Determinants of preferences for genetic counselling in Jewish womenCarmel Apicella, Stuart J Peacock, Lesley Andrews, et al.
Familial Cancer|June 1, 2006
Compliance and Satisfaction with Long-Term Surveillance in Finnish HNPCC FamiliesKirsi Pylvänäinen, Matti Kairaluoma, Jukka-Pekka Mecklin
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