The absence of multiple atypical nevi in germline CDKN2A mutations: Comment on “Hereditary melanoma: Update on syndromes and management: Genetics of familial atypical multiple mole melanoma syndrome”-Reference-Cited by-同舟云学术

The absence of multiple atypical nevi in germline CDKN2A mutations: Comment on “Hereditary melanoma: Update on syndromes and management: Genetics of familial atypical multiple mole melanoma syndrome”

Published:2016-10 Issue:4 Volume:75 Page:e157
ISSN:0190-9622
Container-title:Journal of the American Academy of Dermatology
language:en
Short-container-title:Journal of the American Academy of Dermatology

Author:

Ipenburg Norbertus Anton,Gruis Nelleke A.,Bergman Wilma,van Kester Marloes Sophia

Publisher

Elsevier BV

Subject

Dermatology

Reference5 articles.

1. Hereditary melanoma: update on syndromes and management: genetics of familial atypical multiple mole melanoma syndrome;Soura;J Am Acad Dermatol,2016

2. CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families;Gruis;Melanoma Res,1995

3. Clinical and genetic studies in six Dutch kindreds with the dysplastic naevus syndrome;Bergman;Ann Hum Genet,1986

4. The atypical-mole syndrome and predisposition to melanoma;Wachsmuth;N Engl J Med,1998

5. Genotype/phenotype and penetrance studies in melanoma families with germline CDKN2A mutations;Newton Bishop;J Invest Dermatol,2000

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