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Talseth-Palmer, Bente A.

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Whole genome amplification and its impact on CGH array profiles 75 70 3
Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age 97 93 0
MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer 127 122 2
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients 17 15 0
P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation 29 28 2
Genetic variation and its role in malignancy 26 20 3
Copy number variation in hereditary non-polyposis colorectal cancer 38 36 0
Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome 10 9 0
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients 8 8 0
Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility 7 6 0
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Talseth-Palmer, Bente A.

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