Genetic counselling in male carriers of BRCA1 and BRCA2 gene mutations

BRCA1 and BRCA2 gene mutations cause hereditary breast and ovarian cancer syndrome. The disease has autosomal dominant mode of inheritance, and both genders have the same probability of inheriting the trait. However, the phenotype is different in males and females, and the risk of cancer is signific...

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Veröffentlicht in:	Klinická onkologie 2012, Vol.25 Suppl, p.S67-S73
Hauptverfasser:	Plevová, P, Hladíková, A
Format:	Artikel
Sprache:	cze
Schlagworte:	Breast Neoplasms, Male - genetics Female Genes, BRCA1 Genes, BRCA2 Genetic Counseling Genetic Predisposition to Disease Heterozygote Humans Male Mutation Neoplasms - genetics
Online-Zugang:	Volltext
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