Benign Tumors and Non-Melanoma Skin Cancers in Patients with Fanconi Anemia
Clarification of the clinical significance of an intron variant in a case of Peutz–Jeghers syndrome with abnormal RNA splicing of STK11
Coexisting germline variants of MLH1 and MSH6 in a patient with Lynch syndrome, endometrial cancer, and ovarian cancer
Prevalence of Birt-Hogg-Dube Syndrome and Kidney Cancer Surveillance in Tasmania, Australia
Clinician perspectives on policy approaches to genetic risk disclosure in families
Cascade testing in Italian Hereditary Breast Ovarian Cancer families: a missed opportunity for cancer prevention?
A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report
Perspectives on the implications of carrying putative pathogenic variants in the medulloblastoma predisposition genes ELP1 and GPR161
Hereditary acute myeloid leukemia associated with C-terminal CEBPA germline variants
Mainstreamed Genetic Testing of Breast Cancer Patients in Two Hospitals in South Eastern Norway