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Now showing items 1-10 of 18
Analysis of Mismatch Repair Genes in Hereditary Non-Polyposis Colorectal Cancer Patients
Liu, B.; Parsons, R.; Papadopoulos, N.; Nicolaides, N. C.; Lynch, H. T.; Watson, P., et al. (1996). Analysis of Mismatch Repair Genes in Hereditary Non-Polyposis Colorectal Cancer Patients. Nat Med, February 1996, 2(2):169-174. doi: http://dx.doi.org/10.1038/nm0296-169
Genetic Counseling in a Navajo Hereditary Nonpolyposis Colorectal Cancer Kindred
Lynch, H. T.; Drouhard, T.; Vasen, H. F.; Cavalieri, J.; Lynch, J.; Nord, S., et al. (1996). Genetic Counseling in a Navajo Hereditary Nonpolyposis Colorectal Cancer Kindred. Cancer, January 1 1996, 77(1):30-35. doi: http://dx.doi.org/10.1002/(SICI)1097-0142(19960101)77:1<30
Molecular and Immunochemical Analyses of RB1 and Cyclin D1 in Human Ductal Pancreatic Carcinomas and Cell Lines
Huang, L.; Lang, D.; Geradts, J.; Obara, T.; Klein-Szanto, A. J.; Lynch, H. T.; Ruggeri, B. A. (1996). Molecular and Immunochemical Analyses of RB1 and Cyclin D1 in Human Ductal Pancreatic Carcinomas and Cell Lines. Mol Carcinog, February 1996, 15(2):85-95. doi: http://dx.doi.org/10.1002/(SICI)1098-2744(199602)15:2<85
Is there a Role for Prophylactic Subtotal Colectomy among Hereditary Nonpolyposis Colorectal Cancer Germline Mutation Carriers?
Lynch, H. T. (1996). Is there a Role for Prophylactic Subtotal Colectomy among Hereditary Nonpolyposis Colorectal Cancer Germline Mutation Carriers? Dis Colon Rectum, January 1996, 39(1):109-110. doi: http://dx.doi.org/10.1007/BF02048279
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
Linkage Analysis Identifies Gene Carriers among Members of Families with Hereditary Nonpolyposis Colorectal Cancer
Piepoli, A.; Santoro, R.; Cristofaro, G.; Traversa, G. P.; Gennarelli, M.; Accadia, L., et al. (1996). Linkage Analysis Identifies Gene Carriers among Members of Families with Hereditary Nonpolyposis Colorectal Cancer. Gastroenterology, May 1996, 110(5):1404-1409. doi: http://dx.doi.org/10.1053/gast.1996.v110.pm8613044
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
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
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