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Introduction to Special Issue of Familial Cancer

Lynch, H. T.; Snyder, C. L. (2016)

Cancer Genetics

Lynch, H. T.; Boland, C. R. (Elsevier Inc., 2012)

Hereditary nonpolyposis colorectal cancer (Lynch Syndrome) in Argentina: report from a referral hospital register

Vaccaro, C. A.; Bonadeo, F.; Roverano, A. V.; Peltomaki, P.; Bala, S.; Renkonen, E.; Redal, M. A.; Mocetti, E.; Mullen, E.; Ojea-Quintana, G.; Benati, M. L.; Rivello, H. G.; Clark, M. B.; Lynch, J. F.; Lynch, H. T. (2007)

Origins and prevalence of the American Founder Mutation of MSH2

Clendenning, M.; Baze, M. E.; Sun, S.; Walsh, K.; Liyanarachchi, S.; Fix, D.; Schunemann, V.; Comeras, I.; Deacon, M.; Lynch, J. F.; Gong, G.; Thomas, B. C.; Thibodeau, S. N.; Lynch, H. T.; Hampel, H.; De la Chapelle, A. (2008)

Brain tumors in individuals with familial adenomatous polyposis: a cancer registry experience and pooled case report analysis

Attard, T. M.; Giglio, P.; Koppula, S.; Snyder, C.; Lynch, H. T. (2007)

Population differences in familial adenomatous polyposis may be an expression of geographic differences in APC mutation pattern

Attard, T. M.; Young, R. J.; Stoner, J. A.; Lynch, H. T. (2007)

The risk of endometrial cancer in women with BRCA1 and BRCA2 mutations. A prospective study

Beiner, M. E.; Finch, A.; Rosen, B.; Lubinski, J.; Moller, P.; Ghadirian, P.; Lynch, H. T.; Friedman, E.; Sun, P.; Narod, S. A. (2007)

CHEK2 mutation and hereditary breast cancer

Narod, S. A.; Lynch, H. T. (2007)

Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 mutation

Finch, A.; Beiner, M.; Lubinski, J.; Lynch, H. T.; Moller, P.; Rosen, B.; Murphy, J.; Ghadirian, P.; Friedman, E.; Foulkes, W. D.; Kim-Sing, C.; Wagner, T.; Tung, N.; Couch, F.; Stoppa-Lyonnet, D.; Ainsworth, P.; Daly, M.; Pasini, B.; Gershoni-Baruch, R.; Eng, C.; Olopade, O. I.; McLennan, J.; Karlan, B.; Weitzel, J.; Sun, P.; Narod, S. A.; Hereditary Ovarian Canc Clin Study (2006)

Familial B-cell chronic lymphocytic leukemia - Analysis of cytogenetic abnormalities, immunophenotypic profiles, and immunoglobulin heavy chain gene usage

Aoun, P.; Zhou, G.; Chan, W. C.; Page, C.; Neth, K.; Pickering, D.; Sanger, W.; Quinn-Laquer, B.; Watson, P.; Lynch, J. F.; Lynch, H. T.; Weisenburger, D. D. (2007)

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