Characterisation of humanpatchedgerm line mutations in naevoid basal cell carcinoma syndrome
โ Scribed by N. J. Lench; Elizabeth A. R. Telford; Alec S. High; Alexander F. Markham; Carol Wicking; Brandon J. Wainwright
- Publisher
- Springer
- Year
- 1997
- Tongue
- English
- Weight
- 116 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0340-6717
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๐ SIMILAR VOLUMES
Mutations in the human homologue of Drosophila patched (PTCH) have been identified in patients with nevoid basal cell carcinoma syndrome (NBCCS; also called Gorlin syndrome) as well as sporadic basal cell carcinomas and medulloblastomas. However, using PCR-SSCP analysis, mutations in PTCH have been
## Abstract Nevoid basal cell carcinoma syndrome (NBCCS) is characterized by developmental defects and tumorigenesis. The clinical manifestations of NBCCS have been reported in large epidemiological studies from the United States, the United Kingdom, and Australia, but not from an Asian country. We