Sporadic multiple primary melanoma cases:CDKN2Agermline mutations with a founder effect-Reference-Cited by-同舟云学术

Sporadic multiple primary melanoma cases:CDKN2Agermline mutations with a founder effect

Published:2001-08-28 Issue:3 Volume:32 Page:195-202
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosom. Cancer

Author:

Auroy Stéphane,Avril Marie-Françoise,Chompret Agnès,Pham Danièle,Goldstein Alisa M.,Bianchi-Scarrà Giovanna,Frebourg Thierry,Joly Pascal,Spatz Alain,Rubino Carole,Demenais Florence,Bressac-de Paillerets Brigitte,

Funder

AP-HP

Fondation Sanofi Vaincre le Mélanome

Association pour la Recherche contre le Cancer (ARC) Subvention libre 1998

Publisher

Wiley

Subject

Cancer Research,Genetics

Reference37 articles.

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3. Penetrance and expressivity of the chromosome 9 melanoma susceptibility locus (MLM);Cannon-Albright;Cancer Res,1994

4. Genetic aspects of malignant melanoma;Cawley;Arch Dermatol,1952

5. A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families;Ciotti;Am J Hum Genet,2000

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