Mutation analysis of the human homologue ofdrosophila patched and the xeroderma pigmentosum complementation group A genes in squamous cell carcinomas of the skin
- 1 February 1998
- journal article
- Published by Wiley in Molecular Carcinogenesis
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- The role of the human homologue of Drosophila patched in sporadic basal cell carcinomasNature Genetics, 1996
- Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancerBritish Journal of Cancer, 1996
- Human Homolog of patched , a Candidate Gene for the Basal Cell Nevus SyndromeScience, 1996
- Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma SyndromeCell, 1996
- Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomasHuman Molecular Genetics, 1995
- Nevoid Basal Cell Carcinoma SyndromeDermatologic Clinics, 1995
- High frequency of loss of heterozygosity in actinic keratoses, a usually benign diseaseThe Lancet, 1994
- The emerging epidemic of skin cancerBritish Journal of Dermatology, 1994
- Developmental defects in gorlin syndrome related to a putative tumor suppressor gene on chromosome 9Cell, 1992
- Location of gene for Gorlin syndromeThe Lancet, 1992