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Chromosome abnormalities in benign prostatic hyperplasia

✍ Scribed by Magdy S. Aly; Paola Dal Cin; Herman Van Den Berghe; Wim Van De Voorde; Hein Van Poppel; Filip Ameye; Luc Baert

Publisher: John Wiley and Sons
Year: 1994
Tongue: English
Weight: 503 KB
Volume: 9
Category: Article
ISSN: 1045-2257
DOI: 10.1002/gcc.2870090402

No coin nor oath required. For personal study only.

✦ Synopsis

We combined conventional cytogenetic analysis and fluorescence in situ hybridization of short-term cultures of 28 samples from benign prostatic hyperplasia. Lou of the Y chromosome was the most common chromosome change, followed by trisomy 7.

Trisomy 7, however, may be unrelated to the origin of benign prostate hyperplasia, in which the only and not very specific change seems to be the loss of the Y chromosome. Genes Chrom Cancer 9:227-233 (1594).

cinomas, primary and metastatic tumors, as well as

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