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  1. 1
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  2. 2
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  3. 3
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  4. 4
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    K C Johnson, S Pan, Y Mao, Risk factors for male breast cancer in Canada, 1994–1998, European Journal of Cancer Prevention, 2002, 11, 3, 253

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  7. 7
    Agnes B. Baffoe-Bonnie, Terri H. Beaty, Joan E. Bailey-Wilson, Lambertus A.L.M. Kiemeney, Helgi Sigvaldason, Gud̄rid̄ur Ólafsdóttir, Laufey Tryggvadóttir, Hrafn Tulinius, Genetic epidemiology of breast cancer: Segregation analysis of 389 Icelandic pedigrees, Genetic Epidemiology, 2000, 18, 1
  8. 8
    A Dørum, P Møller, E.J Kamsteeg, H Scheffer, M Burton, K.R Heimdal, L.O Mæhle, E Hovig, C.G Tropé, A.H van der Hout, M.A van der Meulen, C.H.C.M Buys, G.J te Meerman, A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing, European Journal of Cancer, 1997, 33, 14, 2390

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  9. 9
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  10. 10
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  11. 11
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  12. 12
    L. ESSIOUX, L. ABEL, C. BONAIÏTI-PELLIÉ, Genetic epidemiology of breast cancer: interest of survival analysis methods, Annals of Human Genetics, 1995, 59, 3
  13. 13
    A. G. McKinley, S. E. H. Russell, R. A. J. Spence, W. Odling-Smee, N. C. Nevin, Hereditary breast cancer and linkage analysis to BRCA1, British Journal of Surgery, 1995, 82, 8
  14. 14
    Ping-Ling Chen, Thomas A. Sellers, Stephen S. Rich, John D. Potter, Aaron R. Folsom, Segregation analysis of breast cancer in a population-based sample of postmenopausal probands: The Iowa women's health study, Genetic Epidemiology, 1995, 12, 4
  15. 15
    Elizabeth B. Claus, Neil Risch, W. Douglas Thompson, Autosomal dominant inheritance of early-onset breast cancer. Implications for risk prediction, Cancer, 1994, 73, 3
  16. 16
    D. E. Porter, B. B. Cohen, M. R. Wallace, E. Smyth, U. Chetty, J. M. Dixon, C. M. Steel, D. C. Carter, Breast cancer incidence, penetrance and survival in probable carriers of BRCA1 gene mutation in families linked to BRCA1 on chromosome 17q12–21, British Journal of Surgery, 1994, 81, 10
  17. 17
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  18. 18
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  19. 19
    David E. Anderson, Michael D. Badzioch, Familial breast cancer risks. Effects of prostate and other cancers, Cancer, 1993, 72, 1
  20. 20
    D. E. Porter, C. M. Steel, B. B. Cohen, M. R. Wallace, A. Carothers, U. Chetty, D. C. Carter, Genetic linkage analysis applied to unaffected women from families with breast cancer can discriminate high- from low-risk individuals, British Journal of Surgery, 1993, 80, 11
  21. 21
    D. E. Porter, B. B. Cohen, M. R. Wallace, A. Carothers, C. M. Steel, Linkage mapping in familial breast cancer: Improved localisation of a susceptibility locus on chromosome 17q12-21, International Journal of Cancer, 1993, 53, 2
  22. 22
    Elizabeth B. Claus, Neil Risch, W. Douglas Thompson, The calculation of breast cancer risk for women with a first degree family history of ovarian cancer, Breast Cancer Research and Treatment, 1993, 28, 2, 115

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  23. 23
    N. Andrieu, F. Clavel, A. Auquier, M.G. Lê, B. Gairard, L. Piana, A. Brémond, J. Lansac, R. Flamant, R. Renaud, Variations in the risk of breast cancer associated with a family history of breast cancer according to age at onset and reproductive factors, Journal of Clinical Epidemiology, 1993, 46, 9, 973

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  24. 24
    R. S. HOULSTON, A. COLLINS, J. SLACK, N. E. MORTON, Dominant genes for colorectal cancer are not rare, Annals of Human Genetics, 1992, 56, 2
  25. 25
    F. CLERGET-DARPOUX, C. BONAÏTI-PELLIÉ, Strategies based on marker information for the study of human diseases, Annals of Human Genetics, 1992, 56, 2
  26. 26
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  27. 27
    N. E. Morton, D. C. Shields, A. Collins, Genetic epidemiology of complex phenotypes, Annals of Human Genetics, 1991, 55, 4
  28. 28
    R. S. Houlston, A. Collins, J. Slack, S. Campbell, W. P. Collins, M. I. Whitehead, N. E. Morton, Genetic epidemiology of ovarian cancer: segregation analysis, Annals of Human Genetics, 1991, 55, 4