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Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing
- Singh, Ashish Kumar, Talseth-Palmer, Bente, Xavier, Alexandre, Scott, Rodney J., Drabløs, Finn, Sjursen, Wenche
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Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer
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The role of modifier genes in Lynch Syndrome
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