Hereditary Cancer In Clinical Practice

A family pedigree of malignancies associated with BRCA1 pathogenic variants: a reflection of the state of art in China

BRACAVENIR: an observational study of expectations and coping in young women with high hereditary risk of breast and ovarian cancer

Outcomes of screening and surveillance in people with two parents affected by colorectal cancers: experiences from the Familial Bowel Cancer Service

Patients with pathogenic variants for breast cancer other than BRCA1 and BRCA2: qualitative interviews about health care experiences

Validation of a digital identification tool for individuals at risk for hereditary cancer syndromes

Somatic variants of potential clinical significance in the tumors of BRCA phenocopies

Frequency of BRCA1 and BRCA2 causative founder variants in ovarian cancer patients in South-East Poland

Selected Abstracts from the 3rd European Hereditary Tumour Group Meeting (EHTG 2018) Abstracts

Germline c.1A > C heterozygous pathogenic variant in SDHA reported for the first time in a young adult with a gastric gastrointestinal stromal tumour (GIST): a case report