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Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia
Uptake of hysterectomy and bilateral salpingooophorectomy in carriers of pathogenic mismatch repair variants
Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT
Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families
Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families
Germline TERT promoter mutations are rare in familial melanoma