Genetics of familial atypical multiple mole-melanoma (FAMMM) syndrome in The Netherlands: how far have we come?

Abstract:

:By the genetic localization of the first melanoma susceptibility gene on chromosome 1p we thought that the puzzle on familial melanoma families would soon be solved. Now, almost fifteen years later we have learned that inherited melanoma is not a simple genetic disorder and that multiple genes, modifying genes and environmental factors might be involved. This paper outlines the current understanding of the genetics of melanoma and the relationship to atypical nevi based on more than ten years of genetic analysis in the Dutch familial atypical multiple mole-melanoma (FAMMM) syndrome families.

journal_name

Bull Cancer

journal_title

Bulletin du cancer

authors

Gruis NA,Van der Velden PA,Bergman W,Frants RR

subject

Has Abstract

pub_date

1998-07-01 00:00:00

pages

627-30

issue

7

eissn

0007-4551

issn

1769-6917

journal_volume

85

pub_type

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