Associated Papers
AXIN2-related oligodontia-colorectal cancer syndrome with cleft palate as a possible new feature.
Roht L et al.
Molecular Genetics & Genomic Medicine, 2023
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.
Leclerc J et al.
Genes, Chromosomes & Cancer, 2023
36502525 (PubMed )
Supplement: GCC-62-210-s001.xlsx › AXIN2_variants
Clinical and genetic characteristics in lymphoma patients with a second solid malignancy.
Zhou D et al.
Frontiers in Oncology, 2023
37546421 (PubMed )
Supplement: DataSheet_1.xlsx › Sheet1
Clinical implications of genetic testing in familial intermediate and late-onset colorectal cancer.
Djursby M et al.
Human Genetics, 2022
Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families.
Van Marcke C et al.
Breast Cancer Research : Bcr, 2020
32295625 (PubMed )
Supplement: 13058_2020_1273_MOESM1_ESM.xlsx › Table_S2
Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing.
Dominguez-Valentin M et al.
Scientific Reports, 2019
31811167 (PubMed )
Supplement: 41598_2019_54517_MOESM3_ESM.xlsx › Sheet1
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