CDKN2a/p16INK4a Mutations and Lack of p19ARF Involvement in Familial Melanoma Kindreds-Reference-Cited by-同舟云学术

CDKN2a/p16INK4a Mutations and Lack of p19ARF Involvement in Familial Melanoma Kindreds

Published:1998-12 Issue:6 Volume:111 Page:1202-1206
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Fargnoli Maria Concetta,Chimenti Sergio,Peris Ketty,Keller Gisela,Soyer Hans Peter,Pozzo Vera Dal,Höfler Heinz

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference44 articles.

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3. Rates of p16 (MTS1) mutations in primary tumours with 9p21 loss;Cairns;Nature,1994

4. Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma;Caldas;Nature Genet,1994

5. Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22;Cannon-Albright;Science,1992

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