Localization of a Novel Melanoma Susceptibility Locus to 1p22

This publication has 42 references indexed in Scilit:

• Geographical Variation in the Penetrance of CDKN2A Mutations for Melanoma
  JNCI Journal of the National Cancer Institute, 2002
• Genotype/Phenotype and Penetrance Studies in Melanoma Families with Germline CDKN2A Mutations
  Journal of Investigative Dermatology, 2000
• Melanocortin-1 Receptor Polymorphisms and Risk of Melanoma: Is the Association Explained Solely by Pigmentation Phenotype?
  American Journal of Human Genetics, 2000
• Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group [published erratum appears in Hum Mol Genet 1998 May;7(5):941]
  Human Molecular Genetics, 1998
• Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds
  Nature Genetics, 1995
• Linkage mapping of melanoma (MLM) using 172 microsatellite markers
  Genomics, 1992
• The Dutch FAMMM family material: Clinical and genetic data
  Cytogenetic and Genome Research, 1992
• Exclusion of the familial melanoma locus (MLM) from the PNDD1S47 and MYCL1 regions of chromosome arm 1p in 7 Australian pedigrees
  Genomics, 1992
• Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21
  Science, 1990
• Mapping the Gene for Hereditary Cutaneous Malignant Melanoma–Dysplastic Nevus to Chromosome Lp
  New England Journal of Medicine, 1989