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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:
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Citation: B. Modan et al., Parity, oral contraceptives, and the risk of ovarian cancer among carriersand noncarriers of a BRCA1 or BRCA2 mutation, N ENG J MED, 345(4), 2001, pp. 235-240
Authors:
Goldstein, AM
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Citation: Am. Goldstein et al., A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families, BR J CANC, 85(4), 2001, pp. 527-530
Authors:
Goldstein, AM
Struewing, JP
Chidambaram, A
Fraser, MC
Tucker, MA
Citation: Am. Goldstein et al., Genotype-phenotype relationships in US melanoma-prone families with CDKN2Aand CDK4 mutations, J NAT CANC, 92(12), 2000, pp. 1006-1010
Authors:
Lakhani, SR
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Citation: Sr. Lakhani et al., The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2, CLIN CANC R, 6(3), 2000, pp. 782-789
Authors:
Biesecker, BB
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Hadley, DW
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Citation: Bb. Biesecker et al., Psychosocial factors predicting BRCA1/BRCA2 testing decisions in members of hereditary breast and ovarian cancer families, AM J MED G, 93(4), 2000, pp. 257-263
Authors:
Fishman, A
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Chetrit, A
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Beck, D
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Piura, B
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Citation: A. Fishman et al., Patients with double primary tumors in the breast and ovary - Clinical characteristics and BRCA1-2 mutations status, GYNECOL ONC, 79(1), 2000, pp. 74-78
Authors:
Sherman, ME
Lee, JS
Burks, RT
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Hartge, P
Citation: Me. Sherman et al., Histopathologic features of ovaries at increased risk for carcinoma - A case-control analysis, INT J GYN P, 18(2), 1999, pp. 151-157