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Familial Cancer|June 1, 2006
A 'nonsense' mutation leads to aberrant splicing of hMLH1 in a German hereditary non-polyposis colorectal cancer familyJ Baehring, C Sutter, M Kadmon, et al.Familial Cancer|May 27, 2010
Breast cancer susceptibility variants alter risk in familial ovarian cancerA Latif, H J McBurney, S A Roberts, et al.Familial Cancer|May 25, 2010
Magnetic resonance colonography for colorectal cancer screening in patients with Lynch syndrome gene mutationEu Jin Lim, Christopher Leung, Alex Pitman, et al.Familial Cancer|May 18, 2010
Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testingCourtney Doughty Rice, Jennifer Gamm Ruschman, Lisa J Martin, et al.Familial Cancer|September 28, 2010
Hereditary prostate cancer as a feature of Lynch syndromeChristina M Bauer, Anna M Ray, Bronwen A Halstead-Nussloch, et al.Familial Cancer|June 23, 2010
Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer familiesSzilvia Solyom, Katri Pylkäs, Robert WinqvistFamilial Cancer|August 25, 2010
Thymoma associated with malignancies may herald a hereditary cancer syndromeOmid Saeed Tehrani, Emily Q Chen, David L Schaebler, et al.Familial Cancer|August 17, 2010
Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidenceEva Esteban Cardeñosa, Pascual Bolufer Gilabert, Inmaculada de Juan Jiménez, et al.Familial Cancer|August 10, 2010
Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancerLuca Cavallone, Suzanna L Arcand, Christine M Maugard, et al.Familial Cancer|June 21, 2008
Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome populationMef Nilbert, Friedrik P Wikman, Thomas V O Hansen, et al.Pageof 151