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Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study.
Neuhausen SL, Mazoyer S, Friedman L, Stratton M, Offit K, Caligo A, Tomlinson G, Cannon-Albright L, Bishop T, Kelsell D, Solomon E, Weber B, Couch F, Struewing J, Tonin P, Durocher F, Narod S, Skolnick MH, Lenoir G, Serova O, Ponder B, Stoppa-Lyonnet D, Easton D, King MC, Goldgar DE. Neuhausen SL, et al. Among authors: solomon e. Am J Hum Genet. 1996 Feb;58(2):271-80. Am J Hum Genet. 1996. PMID: 8571953 Free PMC article.
Genetic heterogeneity of early-onset familial breast cancer.
Sobol H, Mazoyer S, Narod SA, Smith SA, Black DM, Kerbrat P, Jamot B, Solomon E, Ponder BA, Guerin D. Sobol H, et al. Among authors: solomon e. Hum Genet. 1992 Jun;89(4):381-3. doi: 10.1007/BF00194307. Hum Genet. 1992. PMID: 1352270
Genetics and cancer.
Cavenee WK, Ponder B, Solomon E. Cavenee WK, et al. Among authors: solomon e. Eur J Cancer. 1991;27(12):1706-7. doi: 10.1016/0277-5379(91)90451-i. Eur J Cancer. 1991. PMID: 1782088 No abstract available.
Genetic, functional, and histopathological evaluation of two C-terminal BRCA1 missense variants.
Lovelock PK, Healey S, Au W, Sum EY, Tesoriero A, Wong EM, Hinson S, Brinkworth R, Bekessy A, Diez O, Izatt L, Solomon E, Jenkins M, Renard H, Hopper J, Waring P, Tavtigian SV, Goldgar D, Lindeman GJ, Visvader JE, Couch FJ, Henderson BR, Southey M, Chenevix-Trench G, Spurdle AB, Brown MA; kConFab Investigators. Lovelock PK, et al. Among authors: solomon e. J Med Genet. 2006 Jan;43(1):74-83. doi: 10.1136/jmg.2005.033258. Epub 2005 May 27. J Med Genet. 2006. PMID: 15923272 Free PMC article.
1,133 results