| Literature DB >> 8527383 |
T Dijkhuizen1, E van den Berg, M Wilbrink, M Weterman, A Geurts van Kessel, S Störkel, R P Folkers, A Braam, B de Jong.
Abstract
Several human renal cell carcinomas with X;autosome translocations have been reported in recent years. The t(X;1)(p11.2;q21) appears to be a specific primary anomaly, suggesting that tumors with this translocation form a distinct subgroup of RCC. Here we report two new cases, one with a t(X;10)(p11.2;q23), the other with a t(X;1)(p11.2;p34). The common breakpoint in Xp11.2 suggests that they belong to the above-mentioned subset of RCC. Using FISH in conjunction with X-specific YAC clones, we demonstrate that the two new cases exhibited distinct breakpoints within Xp11.2.Entities:
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Year: 1995 PMID: 8527383 DOI: 10.1002/gcc.2870140108
Source DB: PubMed Journal: Genes Chromosomes Cancer ISSN: 1045-2257 Impact factor: 5.006