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Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study.
Neuhausen SL, Godwin AK, Gershoni-Baruch R, Schubert E, Garber J, Stoppa-Lyonnet D, Olah E, Csokay B, Serova O, Lalloo F, Osorio A, Stratton M, Offit K, Boyd J, Caligo MA, Scott RJ, Schofield A, Teugels E, Schwab M, Cannon-Albright L, Bishop T, Easton D, Benitez J, King MC, Ponder BA, Weber B, Devilee P, Borg A, Narod SA, Goldgar D. Neuhausen SL, et al. Among authors: Osorio A. Am J Hum Genet. 1998 Jun;62(6):1381-8. doi: 10.1086/301885. Am J Hum Genet. 1998. PMID: 9585613 Free PMC article.
Prevalence of BRCA1 and BRCA2 Jewish mutations in Spanish breast cancer patients.
Díez O, Osorio A, Robledo M, Barroso A, Domènech M, Cortés J, Albertos J, Sanz J, Brunet J, SanRomán JM, Alonso MC, Baiget M, Benítez J. Díez O, et al. Among authors: Osorio A. Br J Cancer. 1999 Mar;79(7-8):1302-3. doi: 10.1038/sj.bjc.6690208. Br J Cancer. 1999. PMID: 10098775 Free PMC article.
Genetic and clinical analysis in 10 Spanish patients with multiple endocrine neoplasia type 1.
Cebrián A, Herrera-Pombo JL, Díez JJ, Sánchez-Vilar O, Lara JI, Vázquez C, Picó A, Osorio A, Martínez-Delgado B, Benítez J, Robledo M. Cebrián A, et al. Among authors: Osorio A. Eur J Hum Genet. 1999 Jul;7(5):585-9. doi: 10.1038/sj.ejhg.5200336. Eur J Hum Genet. 1999. PMID: 10439966
Three novel RDS-peripherin mutations (689delT, 857del17, G208D) in Spanish families affected with autosomal dominant retinal degenerations. Mutations in brief no. 147. Online.
Trujillo MJ, Bueno J, Osorio A, Sanz R, Garcia-Sandoval B, Ramos C, Ayuso C. Trujillo MJ, et al. Among authors: Osorio A. Hum Mutat. 1998;12(1):70. doi: 10.1002/(SICI)1098-1004(1998)12:1<70::AID-HUMU13>3.0.CO;2-G. Hum Mutat. 1998. PMID: 10627133
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