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The Breast Journal|September 25, 2009
Family information service participation increases the rates of mutation testing among members of families with BRCA1/2 mutationsHenry T Lynch, Carrie L Snyder, Jane F Lynch, et al.
American Journal of Medical Genetics|October 31, 2002
Hereditary chronic lymphocytic leukemia: an extended family study and literature reviewHenry T Lynch, Dennis D Weisenburger, Brigid Quinn-Laquer, et al.
Cancer Genetics and Cytogenetics|October 23, 2008
Genetic counseling for DAPK1 mutation in a chronic lymphocytic leukemia familyHenry T Lynch, Kelly M Ferrara, Dennis D Weisenburger, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 10, 2007
Who should be sent for genetic testing in hereditary colorectal cancer syndromes?Henry T Lynch, C Richard Boland, Miguel A Rodriguez-Bigas, et al.
Cancer Genetics and Cytogenetics|January 22, 2004
Challenging colonic polyposis pedigrees: differential diagnosis, surveillance, and management concernsHenry T Lynch, Susan T Tinley, Trudy G Shaw, et al.
Molecular Oncology|April 23, 2009
Hereditary ovarian carcinoma: heterogeneity, molecular genetics, pathology, and managementHenry T Lynch, Murray Joseph Casey, Carrie L Snyder, et al.
Cancer Genetics and Cytogenetics|March 11, 2006
Patient responses to the disclosure of BRCA mutation tests in hereditary breast-ovarian cancer familiesHenry T Lynch, Carrie Snyder, Jane F Lynch, et al.
Cancer Genetics and Cytogenetics|October 16, 2002
Family with acute myelocytic leukemia, breast, ovarian, and gastrointestinal cancerHenry T Lynch, Dennis D Weisenburger, Brigid Quinn-Laquer, et al.
European Journal of Human Genetics : EJHG|February 16, 2006
Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implicationsHenry T Lynch, C Richard Boland, Gordon Gong, et al.
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