| Literature DB >> 8938443 |
M Miozzo1, D Perotti, F Minoletti, P Mondini, S Pilotti, R Luksch, F Fossati-Bellani, M A Pierotti, G Sozzi, P Radice.
Abstract
Different findings suggest that alterations of chromosome 7 genes play a role in the development of Wilms tumors. To define the positions of these genes, we have accomplished a combined cytogenetic and molecular study on 11 sporadic Wilms tumors. In one case, where both chromosomes 7 were rearranged, the karyotypic picture was consistent with the presence of a tumor suppressor gene at 7p15. To test this hypothesis, a loss of heterozygosity analysis was performed using microsatellite markers. This revealed a common region of allele losses mapped to the proximal short arm of chromosome 7 and defined the position of the gene(s) involved in Wilms tumors within an interval of approximately 25 cM.Entities:
Mesh:
Year: 1996 PMID: 8938443 DOI: 10.1006/geno.1996.0565
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736