Familial Cancer

Development and pilot testing of a leaflet informing women with breast cancer about genomic testing for polygenic risk

Risk management adherence following genetic testing for hereditary cancer syndromes: a Singaporean experience

RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers

Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene

Genetic counseling referral for ovarian cancer patients: a call to action

Pediatric craniopharyngioma in association with familial adenomatous polyposis

Quality of life following prophylactic gynecological surgery: experiences of female Lynch mutation carriers

APC mosaicism in a young woman with desmoid type fibromatosis and familial adenomatous polyposis

Referral frequency, attrition rate, and outcomes of germline testing in patients with pancreatic adenocarcinoma

Potentially pathogenic germline CHEK2 c.319+2T > A among multiple early-onset cancer families