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Now showing items 1-10 of 18
Clinical and Pathological Features of Ovarian Cancer in Women with Germ-Line Mutations of BRCA1
Rubin, S. C.; Benjamin, I.; Behbakht, K.; Takahashi, H.; Morgan, M. A.; LiVolsi, V. A., et al. (1996). Clinical and Pathological Features of Ovarian Cancer in Women with Germ-Line Mutations of BRCA1. N Engl J Med, November 7 1996, 335(19):1413-1416. doi: http://dx.doi.org/10.1056/NEJM199611073351901
Autonomy of the Epithelial Phenotype in Human Ovarian Surface Epithelium: Changes with Neoplastic Progression and with a Family History of Ovarian Cancer
Dyck, H. G.; Hamilton, T. C.; Godwin, A. K.; Lynch, H. T.; Maines-Bandiera, S.; Auersperg, N. (1996). Autonomy of the Epithelial Phenotype in Human Ovarian Surface Epithelium: Changes with Neoplastic Progression and with a Family History of Ovarian Cancer. Int J Cancer, December 20 1996, 69(6):429-436. doi: http://dx.doi.org/10.1002/(SICI)1097-0215(19961220)69:6<429
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 Syndromes
Moore, S. K.; Zambrano, N.; Lynch, H. T.; Lipkin, M.; Kopelovich, L. (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 Syndromes. Cancer Genet Cytogenet, September 1996, 90(2):125-129. doi: http://dx.doi.org/10.1016/S0165-4608(96)00072-6
Microscopic Benign and Invasive Malignant Neoplasms and a Cancer-Prone Phenotype in Prophylactic Oophorectomies
Salazar, H.; Godwin, A. K.; Daly, M. B.; Laub, P. B.; Hogan, W. M.; Rosenblum, N., et al. (1996). Microscopic Benign and Invasive Malignant Neoplasms and a Cancer-Prone Phenotype in Prophylactic Oophorectomies. J Natl Cancer Inst, December 18 1996, 88(24):1810-1820. doi: http://dx.doi.org/10.1093/jnci/88.24.1810
Molecular Genetic Evidence of the Occurrence of Breast Cancer as an Integral Tumor in Patients with the Hereditary Nonpolyposis Colorectal Carcinoma Syndrome
Risinger, J. I.; Barrett, J. C.; Watson, P.; Lynch, H. T.; Boyd, J. (1996). Molecular Genetic Evidence of the Occurrence of Breast Cancer as an Integral Tumor in Patients with the Hereditary Nonpolyposis Colorectal Carcinoma Syndrome. Cancer, May 1 1996, 77(9):1836-1843. doi: http://dx.doi.org/10.1002/(SICI)1097-0142(19960501)77:9<1836
A Polymorphic Stop Codon in BRCA2
Mazoyer, S.; Dunning, A. M.; Serova, O.; Dearden, J.; Puget, N.; Healey, C. S., et al. (1996). A Polymorphic Stop Codon in BRCA2. Nat Genet, November 1996, 14(3):253-254. doi: http://dx.doi.org/10.1038/ng1196-253
Muir-Torre Syndrome and Defective DNA Mismatch Repair Genes
Fusaro, R. M.; Lemon, S. J.; Lynch, H. T. (1996). Muir-Torre Syndrome and Defective DNA Mismatch Repair Genes. J Am Acad Dermatol, September 1996, 35(3 Part 1):493-494. doi: http://dx.doi.org/10.1016/S0190-9622(96)90644-1
Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome). an Updated Review
Lynch, H. T.; Smyrk, T. (1996). Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome). an Updated Review. Cancer, September 15 1996, 78(6):1149-1167. doi: http://dx.doi.org/10.1002/(SICI)1097-0142(19960915)78:6<1149
Ovarian Cancer Risk in BRCA1 Carriers is Modified by the HRAS1 Variable Number of Tandem Repeat (VNTR) Locus
Phelan, C. M.; Rebbeck, T. R.; Weber, B. L.; Devilee, P.; Ruttledge, M. H.; Lynch, H. T., et al. (1996). Ovarian Cancer Risk in BRCA1 Carriers is Modified by the HRAS1 Variable Number of Tandem Repeat (VNTR) Locus. Nat Genet, March 1996, 12(3):309-311. doi: http://dx.doi.org/10.1038/ng0396-309
Hereditary Breast Cancer: Pathobiology, Prognosis, and BRCA1 and BRCA2 Gene Linkage
Marcus, J. N.; Watson, P.; Page, D. L.; Narod, S. A.; Lenoir, G. M.; Tonin, P., et al. (1996). Hereditary Breast Cancer: Pathobiology, Prognosis, and BRCA1 and BRCA2 Gene Linkage. Cancer, February 15 1996, 77(4):697-709. doi: http://dx.doi.org/10.1002/(SICI)1097-0142(19960215)77:4<697