Article
Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients.
Human molecular genetics - 1 Mar 1994
Bonifas J M, Bare J W, Kerschmann R L, Master S P, Epstein E H
Abstract excerpt
The basal cell nevus syndrome is an autosomal dominant disease, one of the most prominent phenotypic features of which is a large number of cutaneous basal cell carcinomas. The gene whose mutation underlies this disease has been mapped to chromosome 9q22.3-q31, and basal cell carcinomas frequently have allelic losses including this site. We report here that the chromosome 9q22.3-q31 lost in 24 basal cell...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
