Resumen
The human gene XPC (formerly designated XPCC), which corrects the repair deficiency of xeroderma pigmentosum (XP) group C cells, was mapped to 3p25. A cDNA probe for Southern blot hybridization and diagnostic PCR analyses of hybrid clone panels informative for human chromosomes in general and portions of chromosome 3 in particular produced the initial results. Fluorescence in situ hybridization utilizing both a yeast artificial chromosome DNA containing the gene and XPC cDNA as probes provided verification and specific regional assignment. A conflicting assignment of XPC to chromosome 5 is discussed in light of inadequacies in the exclusive use of microcell-mediated chromosome transfer for gene mapping.
| Idioma original | English (US) |
|---|---|
| Páginas (desde-hasta) | 266-269 |
| Número de páginas | 4 |
| Publicación | Genomics |
| Volumen | 21 |
| N.º | 1 |
| DOI | |
| Estado | Published - may 1 1994 |
ASJC Scopus subject areas
- Genetics
Huella
Profundice en los temas de investigación de 'Assignment of xeroderma pigmentosum group c (xpc) gene to chromosome 3p25'. En conjunto forman una huella única.Citar esto
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