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References
Papadopoulos, N. & Lindblom, A. A. Hum. Mutat. (in the press).
Bronner, C.E. et al. Nature 368, 258–261 (1994).
Tannergard, P. et al. Cancer Res. 55, 6092–6096 (1995).
Parsons, R. et al. Cell 75, 1227–1236 (1993).
Aaltonen, L.A. et al. Science 260, 812–815 (1993).
Hemminki, A. et al. Nature Genet. 8, 405–410 (1994).
Baker, S.M. et al. Nature Genet. 13, 336–342 (1996).
Edelman, W. et al. Cell 85, 1125–1134 (1996).
Parsons, R. et al. Science 268, 738–740 (1995).
Eshleman, J.R. et al. Oncogene 10, 33–37 (1995).
Albertini, R.J. et al. Proc. Natl. Acad. Sci. USA 79, 6617–6621 (1982).
Hou, S.M. et al. Envir. Mol. Mut 25, 97–105 (1995).
Watson, P. & Lynch, H.T. Cancer 71, 677–685 (1993).
Wooster, R. et al. Nature Genet. 6, 152–156 (1994).
Risinger, J.I., Barrett, J.C., Watson, R., Lynch, H.T. & Boyd, J. Cancer 77, 1836–1843 (1996).
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Hackman, P., Tannergård, P., Osei-Mensa, S. et al. A human compound heterozygote for two MLH1 missense mutations. Nat Genet 17, 135–136 (1997). https://doi.org/10.1038/ng1097-135
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DOI: https://doi.org/10.1038/ng1097-135
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