Mutation analysis of the human homologue ofdrosophila patched and the xeroderma pigmentosum complementation group A genes in squamous cell carcinomas of the skin

This publication has 17 references indexed in Scilit:

• The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas
  Nature Genetics, 1996
• Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer
  British Journal of Cancer, 1996
• Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome
  Published by Elsevier ,1996
• Human Homolog of patched , a Candidate Gene for the Basal Cell Nevus Syndrome
  Science, 1996
• Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas
  Human Molecular Genetics, 1995
• Nevoid Basal Cell Carcinoma Syndrome
  Dermatologic Clinics, 1995
• High frequency of loss of heterozygosity in actinic keratoses, a usually benign disease
  The Lancet, 1994
• The emerging epidemic of skin cancer
  British Journal of Dermatology, 1994
• Developmental defects in gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
  Published by Elsevier ,1992
• Location of gene for Gorlin syndrome
  The Lancet, 1992