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Results: 1-7 |
Results: 7

Authors: Wang, WW Spurdle, AB Kolachana, P Bove, B Modan, B Ebbers, SM Suthers, G Tucker, MA Kaufman, DJ Doody, MM Tarone, RE Daly, M Levavi, H Pierce, H Chetrit, A Yechezkel, GH Chenevix-Trench, G Offit, K Godwin, AK Struewing, JP
Citation: Ww. Wang et al., A single nucleotide polymorphism in the 5 ' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers, CANC EPID B, 10(9), 2001, pp. 955-960

Authors: Meiser, B Butow, PN Barratt, AL Schnieden, V Gattas, M Kirk, J Gaff, C Suthers, G Tucker, K
Citation: B. Meiser et al., Long-term outcomes of genetic counseling in women at increased risk of developing hereditary breast cancer, PAT EDUC C, 44(3), 2001, pp. 215-225

Authors: Meiser, B Butow, P Friedlander, M Schnieden, V Gattas, M Kirk, J Suthers, G Haan, E Tucker, K
Citation: B. Meiser et al., Intention to undergo prophylactic bilateral mastectomy in women at increased risk of developing hereditary breast cancer, J CL ONCOL, 18(11), 2000, pp. 2250-2257

Authors: Siah, SP Quinn, DM Bennett, GD Casey, G Flower, RLP Suthers, G Rudzki, Z Rudzki, Z
Citation: Sp. Siah et al., Microsatellite instability markers in breast cancer: A review and study showing MSI was not detected at 'BAT 25' and 'BAT 26' microsatellite markers in early-onset breast cancer, BREAST CANC, 60(2), 2000, pp. 135-142

Authors: Meiser, B Butow, P Barratt, A Suthers, G Smith, M Colley, A Thompson, E Tucker, K
Citation: B. Meiser et al., Attitudes to genetic testing for breast cancer susceptibility in women at increased risk of developing hereditary breast cancer, J MED GENET, 37(6), 2000, pp. 472-476

Authors: Meiser, B Butow, P Barratt, A Friedlander, M Gattas, M Kirk, J Suthers, G Walpole, I Tucker, K
Citation: B. Meiser et al., Attitudes toward prophylactic oophorectomy and screening utilization in women at increased risk of developing hereditary breast/ovarian cancer, GYNECOL ONC, 75(1), 1999, pp. 122-129

Authors: Suthers, G Smith, S Springbett, S
Citation: G. Suthers et al., Skewed sex ratios in familial holoprosencephaly and in people with isolated single maxillary central incisor, J MED GENET, 36(12), 1999, pp. 924-926
Risultati: 1-7 |