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Marjolijn J. L. Ligtenberg et al.
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Marjo van Puijenbroek et al.
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J. Etzler et al.
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High frequency of copy-neutral LOH in MUTYH-associated polyposis carcinomas
A. Middeldorp et al.
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Unbalanced translocation, a major chromosome alteration causing loss of heterozygosity in human lung cancer
H. Ogiwara et al.
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Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patients
M. Spaepen et al.
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H van der Klift et al.
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The 5′ Region of the MSH2 gene involved in hereditary non-polyposis colorectal cancer contains a high density of recombinogenic sequences
FC Charbonnier et al.
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Screening for the Lynch syndrome (Hereditary nonpolyposis colorectal cancer).
H Hampel et al.
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Clinical description of the Lynch syndrome [hereditary nonpolyposis colorectal cancer (HNPCC)]
HFA Vasen
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