Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
Copy number variation in hereditary non-polyposis colorectal cancer
Genetic modifiers of cancer risk in Lynch syndrome: a review
STaRRRT: a table of short tandem repeats in regulatory regions of the human genome
Expanding the genetic basis of copy number variation in familial breast cancer
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