Prior cytogenetic analyses of hepatoblastomas have shown the most common recurring abnormalities to be trisomy for chromosomes 2 and 20, and a recurrent translocation involving chromosomes 1 and 4 identified in a minority of cases. Four cases have shown double minute chromosomes, which provide cytog
Comparative genomic hybridization for genetic analysis of renal oncocytomas
β Scribed by Joseph C. Presti Jr.; Holger Moch; Victor E. Reuter; Danh Huynh; Frederic M. Waldman
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 471 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1045-2257
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β¦ Synopsis
Renal oncocytomas are uncommon tumors of the kidney that are considered to be of low malignant potential. Neither conventional cytogenetic nor restriction fragment length polymorphism analyses have identified consistent genetic alterations in their genomic DNA. The purpose of the present study was to identify the genetic alterations associated with the development of renal oncocytomas. We studied I 3 renal oncocytomas by using comparative genomic hybridization, and we identified loss of genetic material from chromosomes I and/or 14 in six of these tumors. These alterations may represent early genetic events in the development of these tumors.
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