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PCCR: Pancreatic Cancer Collaborative Registry

Sherman, S.; Shats, O.; Ketcham, M. A.; Anderson, M. A.; Whitcomb, D. C.; Lynch, H. T.; Ghiorzo, P.; Rubinstein, W. S.; Sasson, A. R.; Grizzle, W. E.; Haynatzki, G.; Feng, J.; Sherman, A.; Kinarsky, L.; Brand, R. E. (2011)

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.; Lenoir, G. M.; Stratton, M. R.; Easton, D. F.; Ponder, B. A.; Cannon-Albright, L.; Larsson, C.; Goldgar, D. E.; Narod, S. A. (1996)

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.; Linder-Stephenson, L.; Salerno, G.; Conway, T. A.; Lynch, H. T. (1996)

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.; Siena, D.; Bisceglia, M.; Lynch, H. T.; Peltomaki, P.; Andriulli, A. (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

Moore, S. K.; Zambrano, N.; Lynch, H. T.; Lipkin, M.; Kopelovich, L. (1996)

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)

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PCCR: Pancreatic Cancer Collaborative Registry

Ovarian Cancer Risk in BRCA1 Carriers is Modified by the HRAS1 Variable Number of Tandem Repeat (VNTR) Locus

Hereditary Breast Cancer: Pathobiology, Prognosis, and BRCA1 and BRCA2 Gene Linkage

Linkage Analysis Identifies Gene Carriers among Members of Families with Hereditary Nonpolyposis Colorectal Cancer

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

Molecular Genetic Evidence of the Occurrence of Breast Cancer as an Integral Tumor in Patients with the Hereditary Nonpolyposis Colorectal Carcinoma Syndrome

A Polymorphic Stop Codon in BRCA2

Muir-Torre Syndrome and Defective DNA Mismatch Repair Genes

Overview of Natural History, Pathology, Molecular Genetics and Management of HNPCC (Lynch Syndrome)

Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome). an Updated Review

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PCCR: Pancreatic Cancer Collaborative Registry

Ovarian Cancer Risk in BRCA1 Carriers is Modified by the HRAS1 Variable Number of Tandem Repeat (VNTR) Locus

Hereditary Breast Cancer: Pathobiology, Prognosis, and BRCA1 and BRCA2 Gene Linkage

Linkage Analysis Identifies Gene Carriers among Members of Families with Hereditary Nonpolyposis Colorectal Cancer

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

Molecular Genetic Evidence of the Occurrence of Breast Cancer as an Integral Tumor in Patients with the Hereditary Nonpolyposis Colorectal Carcinoma Syndrome

A Polymorphic Stop Codon in BRCA2

Muir-Torre Syndrome and Defective DNA Mismatch Repair Genes

Overview of Natural History, Pathology, Molecular Genetics and Management of HNPCC (Lynch Syndrome)

Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome). an Updated Review