Associated Papers
A novel pathogenic frameshift variant in AXIN2 in a man with polyposis and hypodontia.
Broekema MF et al.
Hereditary Cancer in Clinical Practice, 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
Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancer.
Chan JM et al.
Familial Cancer, 2022
Familial colorectal cancer and tooth agenesis caused by an AXIN2 variant: how do we detect families with rare cancer predisposition syndromes?
Jensen JM et al.
Familial Cancer, 2022
Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene.
Beard C et al.
Familial Cancer, 2019
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