CDKN2A Germline Mutations in U.K. Patients with Familial Melanoma and Multiple Primary Melanomas
- 1 August 1998
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 111 (2) , 269-272
- https://doi.org/10.1046/j.1523-1747.1998.00267.x
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Germline Mutations of the CDKN2 Gene in UK Melanoma FamiliesHuman Molecular Genetics, 1997
- Patients with multiple primary melanomas may have germline CDKN24 mutations and an occult family history of the diseaseMelanoma Research, 1997
- InformativeMspI polymorphism adjacent to exon 3 of thep16INK4(MTS1)geneMolecular and Cellular Probes, 1996
- Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population.Proceedings of the National Academy of Sciences, 1996
- Frequency of homozygous deletion at p16/CDKN2 in primary human tumoursNature Genetics, 1995
- Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindredsNature Genetics, 1995
- Localization of the 9p Melanoma Susceptibility Locus (MLM) to a 2-cM Region between D9S736 and D9S171Genomics, 1994
- Germline p16 mutations in familial melanomaNature Genetics, 1994
- Multiple primary melanoma: risk factors and prognostic implicationsBMJ, 1994
- Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22Science, 1992