Article

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 p16Leiden

2000-09-15

Abstract excerpt

Familial atypical multiple mole melanoma (FAMMM) is an autosomal dominant disease characterized by the familial occurrence of malignant melanoma of the skin and multiple atypical precursor lesions. Germline mutations in the p16 (CDKN2A) gene have been reported in at least a quarter of such families. An association has been reported between p16 mutations and pancreatic cancer. The aim of this study was to assess th...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 7eb72923-341e-5ac8-944e-584e0b537ca1
DOI: 10.1002/1097-0215(20000915)87:6<809::aid-ijc8>3.3.co;2-l

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 p16LeidenDOI 10.1002/1097-0215(20000915)87:6<809::aid-ijc8>3.3.co;2-lRead

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion ofp16 (p16-Leiden)Semantic proximity Read

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden).Semantic proximity Read

Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study.Semantic proximity Read

Novel presentation of a familial pancreatic cancer syndrome.Semantic proximity Read

Development of esophageal squamous cell cancer in patients with FAMMM syndrome: Two clinical reports.Semantic proximity Read

Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variants.Semantic proximity Read

FAMMM syndrome: pathogenesis and management.Semantic proximity Read

Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations.Semantic proximity Read

CDKN2A germline mutations in familial pancreatic cancer.Semantic proximity Read

CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.Semantic proximity Read

A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families.Semantic proximity Read

Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome.Semantic proximity Read