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International Journal of Cancer|December 20, 1996
Autonomy of the epithelial phenotype in human ovarian surface epithelium: changes with neoplastic progression and with a family history of ovarian cancerH G Dyck, T C Hamilton, A K Godwin, et al.Cancer|July 15, 1983
Paravertebral malignant rhabdoid tumor in infancy. In vitro studies of a familial tumorH T Lynch, S B Shurin, B B Dahms, et al.Surgery, Gynecology & Obstetrics|May 1, 1976
Genetic heterogeneity and familial carcinoma of the breastH T Lynch, H A Guirgis, F Brodkey, et al.American Journal of Human Genetics|June 1, 1996
Two distinct origins of a common BRCA1 mutation in breast-ovarian cancer families: a genetic study of 15 185delAG-mutation kindredsD B Berman, J Wagner-Costalas, D C Schultz, et al.Journal of Medical Genetics|February 1, 1983
Phenotypic variation in the familial atypical multiple mole-melanoma syndrome (FAMMM)H T Lynch, R M Fusaro, W A Albano, et al.Patient Education and Counseling|February 13, 2001
Parental communication of BRCA1/2 genetic test results to childrenK P Tercyak, C Hughes, D Main, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 20, 1998
What you don't know can hurt you: adverse psychologic effects in members of BRCA1-linked and BRCA2-linked families who decline genetic testingC Lerman, C Hughes, S J Lemon, et al.Oncology|January 1, 1976
Survival data from a multiphasic mobile cancer detection unitH T Lynch, F D Brodkey, H A Guirgis, et al.Cancer|October 1, 1977
Role of heredity in multiple primary cancerH T Lynch, R E Harris, P M Lynch, et al.Anticancer Research|July 1, 1994
Pathology of hereditary non-polyposis colorectal cancerJ R Jass, T C Smyrk, S M Stewart, et al.Pageof 144