Abstract
A renal cell carcinoma from a 15-year-old male had a 49,Yt(X;1)(p11.2;g21), +der(X)t(X;1) (p11.2;q21), +5, -16, +17, +18 karyotype. This is the third report of a tronslocation involving a breakpoint at Xp11.2 in a renal cell carcinoma in a child. A total of nine cases of renal cell carcinoma involving Xp11, including this case, have been reported. Of the eight cases for which there are genetics reports, all are male. Patients with renal cell carcinoma with abnormalities at Xp11 appear to be younger than renal cell carcinoma patients overall.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 72-75 |
| Number of pages | 4 |
| Journal | Cancer Genetics and Cytogenetics |
| Volume | 81 |
| Issue number | 1 |
| DOIs | |
| State | Published - May 1995 |
ASJC Scopus subject areas
- Genetics
- Molecular Biology
- Cancer Research
Fingerprint
Dive into the research topics of 'Renal cell carcinoma with translocation (X;1) Further evidence for a cytogenetically defined subtype'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS