Associated Papers
Evolutionary origin of germline pathogenic variants in human DNA mismatch repair genes.
Lei H et al.
Human Genomics, 2024
38287404 (PubMed )
Supplement: 40246_2024_573_MOESM3_ESM.xls › PMS2
Functional analysis of clinical BARD1 germline variants.
Toh MR et al.
Cold Spring Harbor Molecular Case Studies, 2019
31371347 (PubMed )
Supplement: supp_mcs.a004093_Supplemental_Materials.docx
A novel MLH1 mutation in a Japanese family with Lynch syndrome associated with small bowel cancer.
Akizawa Y et al.
Human Genome Variation, 2018
Select a paper to view details