Misinterpreting the Results: Patient Misconceptions about Genetic Cancer Risk after Obstetrical Carrier Screening Shortened Title: Perceptions of Genetic Cancer Risk in Prenatal Carrier Screening
Splenic hamartoma in two related patients with BAP1 tumour predisposition syndrome caused by a novel germline BAP1 p.(Gly128Arg) missense variant
Genotypic and Phenotypic Characteristics of Germline TP53 Variant Carriers: Experience from Two Cancer Genetic Counseling Units
Five-year psychological impact and surveillance compliance in the Australian Pancreatic Cancer Screening Program
Beyond 1100delC: Distinct CHEK2 Variants and Unique Cancer Phenotypes in Northeast Brazil
Implementation of Risk-Reducing Surgery for HBOC Under Public Insurance in Japan: A Single-Center Experience
Single Institution Assessment of Compliance with Guideline Directed Aspirin Therapy in the Prevention of Colorectal Cancer in Lynch Syndrome
Cancer Spectrum in Mexican Patients with the CHEK2 p.(Leu236Pro) Variant: A Retrospective Study
5’UTR gene regions in germline DNA sequencing panels: lessons from the analysis of breast and ovarian cancer patients of Tatar and Bashkir ethnic origin
Haplotype analysis detects MLH1 founder variant in Indian Lynch syndrome patient cohort