New developments in melanoma genetics
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology
Link
http://link.springer.com/content/pdf/10.1007/s11912-000-0022-z.pdf
Reference41 articles.
1. Soufir N, Avril MF, Chompret A, et al.: Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France: the French Familial Melanoma Study Group. Hum Mol Genet 1998, 7:209–216.
2. MacKie RM, Andrew N, Lanyon WG, et al.: CDKN2A germline mutations in UK patients with familial melanoma and multiple primary melanomas. J Invest Dermatol 1998, 111:69–272.
3. Kamb A, Shattuck-Eidens D, Eeles R, et al.: Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nat Genet 1994, 8:23–26.
4. Hussussian CJ, Struewing JP, Goldstein AM, et al.: Germline p16 mutations in familial melanoma. Nat Genet 1994, 8:15–21.
5. Newton Bishop JA, Harland M, Bennett DC, et al.: Mutation testing in melanoma families: INK4A, CDK4 and INK4D. Br J Cancer 1999, 80:295–300. CDKN2A mutations were found in eight of 22 (35%) British families with at least three melanoma cases but in only one of 20 (5%) twocase families. The closely related CDKN2D gene was analyzed in 42 UK and 6 US families, but no mutations were found. Similarly, no mutations of the CDK4 gene were detected.
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