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
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
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