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Publication Listing for the MeSH term hereditary. Found 4 abstracts

Ishak MB, Giri VN. A Systematic Review of Replication Studies of Prostate Cancer Susceptibility Genetic Variants in High-Risk Men Originally Identified from Genome-Wide Association Studies. Cancer Epidemiology Biomarkers & Prevention. 2011 Aug;20(8):1599-610.   PMCID: not NIH funded
Locker GY, Kaul K, Weinberg DS, Gatalica Z, Gong G, Peterman A, Lynch J, Klatzco L, Olopade OI, Bomzer CA, Newlin A, Keenan E, Tajuddin M, Knezetic J, Coronel S, Lynch HT. The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features. CANCER GENETICS AND CYTOGENETICS. 2006 Aug;169(1):33-8.
Wang ND, Testa JR, Smith DI. Determination of the Specificity of Aphidicolin-Induced Breakage of the Human-3p14.2 Fragile Site. Genomics. 1993 Aug;17(2):341-7.
Wang ND, Testa JR, Smith DI. Localization of 3 Novel Hybrid Breakpoints and Refinement of 18 Marker Assignments in the Human 3cen-P21.1 Region. Genomics. 1992 Dec;14(4):891-6.
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MeSH cloud from publications including the MeSH term hereditary

Last updated on Saturday, June 06, 2020