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Cancer Genetics and Cytogenetics|September 1, 1996
Absence of germline mutations in exons 5-9 of the p53 gene in patients with Li-Fraumeni-like (SBLA) and familial adenomatous polyposis heritable cancer syndromesS K Moore, N Zambrano, H T Lynch, et al.Cancer|January 15, 1993
Hereditary ovarian cancer. Heterogeneity in age at onsetH T Lynch, P Watson, J F Lynch, et al.Cancer|May 1, 1996
Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndromeJ I Risinger, J C Barrett, P Watson, et al.Cancer Genetics and Cytogenetics|December 1, 1988
Breast cancer diagnosis in a putative obligate gene carrier. A family studyH T Lynch, M L Fitzsimmons, J Schreiman, et al.Gynecologic Oncology|January 1, 1990
Hereditary carcinoma of the ovary and associated cancers: a study of two familiesH T Lynch, M L Fitzsimmons, T A Conway, et al.Cancer Genetics and Cytogenetics|June 1, 1991
Hereditary nonpolyposis colorectal cancer (Lynch syndromes I & II). Genetics, pathology, natural history, and cancer control, Part IH T Lynch, S Lanspa, T Smyrk, et al.European Journal of Cancer (Oxford, England : 1990)|July 1, 1995
Update on the differential diagnosis, surveillance and management of hereditary non-polyposis colorectal cancerH T Lynch, T Smyrk, J Lynch, et al.British Journal of Cancer|June 1, 1990
Systemic cancer and the FAMMM syndromeW Bergman, P Watson, J de Jong, et al.Cancer|July 15, 1987
Family history of colorectal cancer as a marker of potential malignancy within a screening programP Rozen, Z Fireman, A Figer, et al.Surgery, Gynecology & Obstetrics|October 1, 1975
Family studies of malignant melanoma and associated cancerH T Lynch, B C Frichot, P Lynch, et al.Pageof 37