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Published in 2021 at "Cancer genetics"
DOI: 10.1016/j.cancergen.2021.07.002
Abstract: Lynch syndrome (LS) is an autosomal dominant cancer predisposition syndrome defined molecularly by the presence of a pathogenic heterozygous variant in one of the mismatch repair genes: MLH1, MSH2, MSH6, PMS2, or EPCAM. The incidence of LS…
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Keywords:
pediatric spectrum;
defining pediatric;
syndrome defining;
cancer ... See more keywords