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Now showing items 1-10 of 164

American founder mutation for Lynch syndrome: Prevalence estimates and implications

Lynch, H. T.; de la Chapelle, A.; Hampel, H.; Wagner, A.; Fodde, R.; Lynch, J. F.; Okimoto, R.; Clark, M. B.; Coronel, S.; Trowonou, A.; Fu, Y. X.; Haynatzki, G. R.; Gong, G. (2006)

Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications

Lynch, H. T.; Boland, C. R.; Gong, G.; Shaw, T. G.; Lynch, P. M.; Fodde, R.; Lynch, J. F.; de la Chapelle, A. (2006)

Genetics, natural history, and DNA-based counseling in hereditary breast cancer

Lynch, H. T.; Lynch, J. F. (B. C. Decker, 2006)

Genetic disorders associated with exocrine and endocrine pancreatic tumors.

Lynch, H. T.; Deters, C. A.; Lynch, J. F.; Brand, R. (CRC Press, 2006)

Hereditary colorectal cancer: An updated review. Part II: Lynch syndrome (hereditary nonpolyposis colorectal cancer

Lynch, H. T.; Jass, J.; Lynch, J. F.; Attard, T. (2005)

Hereditary colorectal cancer: An updated review. Part I: Hereditary polyposis syndromes

Lynch, H. T.; Jass, J.; Lynch, J. F.; Attard, T. (2005)

Familial myeloma

Lynch, H. T.; Ferrara, K.; Barlogie, B.; Coleman, E. A.; Lynch, J. F.; Weisenburger, D.; Sanger, W.; Watson, P.; Nipper, H.; Witt, V.; Thomé, S. (2008)

Genetic counseling for DAPK1 mutation in a chronic lymphocytic leukemia family

Lynch, H. T.; Ferrara, K. M.; Weisenburger, D. D.; Sanger, W. G.; Lynch, J. F.; Thomé, S. D. (2008)

Predominance of brain tumors in an extended Li-Fraumeni (SBLA) kindred, including a case of Sturge-Weber syndrome

Lynch, H. T.; McComb, R. D.; Osborn, N. K.; Wolpert, P. A.; Lynch, J. F.; Wszolek, Z. K.; Sidransky, D.; Steg, R. E. (2000)

Familial sarcoma - Challenging pedigrees

Lynch, H. T.; Deters, C. A.; Hogg, D.; Lynch, J. F.; Kinarsky, Y.; Gatalica, Z. (2003)

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