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Familial Cancer|October 30, 2012
Value of bilateral breast cancer for identification of rare recessive at-risk alleles: evidence for the role of homozygous GEN1 c.2515_2519delAAGTT mutationEkatherina Sh Kuligina, Anna P Sokolenko, Nathalia V Mitiushkina, et al.
Familial Cancer|November 3, 2012
The deletion of exons 3-5 of BRCA1 is the first founder rearrangement identified in breast and/or ovarian cancer Spanish familiesSarai Palanca, Inmaculada de Juan, Gema Perez-Simó, et al.
Familial Cancer|February 19, 2015
Polymorphisms of the XRCC1 gene and breast cancer risk in the Mexican populationNelly M Macías-Gómez, Valeria Peralta-Leal, Juan Pablo Meza-Espinoza, et al.
Familial Cancer|May 28, 2014
Association of interleukin-23 receptor gene polymorphisms with risk of bladder cancer in ChineseTielong Tang, Hui Xue, Shu Cui, et al.
Familial Cancer|March 31, 2015
Implementing a telephone based peer support intervention for women with a BRCA1/2 mutationAshley Farrelly, Victoria White, Mary-Anne Young, et al.
Familial Cancer|November 25, 2025
Pancreatic cancer surveillance not recommended for familial adenomatous polyposis: a fine and gray risk analysisAleksander M Bogdanski, Derk C F Klatte, Sobia I Laghari, et al.
Familial Cancer|November 26, 2025
Updated genetic testing in individuals with unexplained adenomatous polyposis and the diagnostic yieldBlake Rowell, Maegan E Roberts, Pamela L Brock, et al.
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