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BRCA1 and BRCA2 whole cDNA analysis in unsolved hereditary breast/ovarian cancer patients.
Montalban G, Bonache S, Bach V, Gisbert-Beamud A, Tenés A, Moles-Fernández A, López-Fernández A, Carrasco E, Balmaña J, Diez O, Gutiérrez-Enríquez S. Montalban G, et al. Among authors: diez o. Cancer Genet. 2021 Nov;258-259:10-17. doi: 10.1016/j.cancergen.2021.06.003. Epub 2021 Jun 18. Cancer Genet. 2021. PMID: 34237702
The variant E233G of the RAD51D gene could be a low-penetrance allele in high-risk breast cancer families without BRCA1/2 mutations.
Rodríguez-López R, Osorio A, Ribas G, Pollán M, Sánchez-Pulido L, de la Hoya M, Ruibal A, Zamora P, Arias JI, Salazar R, Vega A, Martínez JI, Esteban-Cardeñosa E, Alonso C, Letón R, Urioste Azcorra M, Miner C, Armengod ME, Carracedo A, González-Sarmiento R, Caldés T, Díez O, Benítez J. Rodríguez-López R, et al. Among authors: diez o. Int J Cancer. 2004 Jul 20;110(6):845-9. doi: 10.1002/ijc.20169. Int J Cancer. 2004. PMID: 15170666 Free article.
Mutant BRCA1 alleles transmission: different approaches and different biases.
de la Hoya M, Meijers-Heijboer H, Fernández JM, Díez O, Osorio A, Alonso C, van Leeuwen I, Díaz-Rubio E, Cornelisse C, Benítez J, Devilee P, Caldés T. de la Hoya M, et al. Among authors: diez o. Int J Cancer. 2005 Jan 1;113(1):166-7. doi: 10.1002/ijc.20541. Int J Cancer. 2005. PMID: 15386425 Free article.
218 results