CHROMOSOME-ABNORMALITIES IN BENIGN PROSTATIC HYPERPLASIA

被引：27

作者：

ALY, MS

DALCIN, P

VANDEVOORDE, W

VANPOPPEL, H

AMEYE, F

BAERT, L

VANDENBERGHE, H

机构：

[1] CATHOLIC UNIV LEUVEN,CTR HUMAN GENET,HERESTR 49,B-3000 LOUVAIN,BELGIUM

[2] CATHOLIC UNIV LEUVEN,DEPT PATHOL,B-3000 LOUVAIN,BELGIUM

[3] CATHOLIC UNIV LEUVEN,DEPT UROL,B-3000 LOUVAIN,BELGIUM

来源：

GENES CHROMOSOMES & CANCER | 1994年 / 9卷 / 04期

关键词：

D O I：

10.1002/gcc.2870090402

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

We combined conventional cytogenetic analysis and fluorescence in situ hybridization of short-term cultures of 28 samples from benign prostatic hyperplasia. Loss 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. (C) 1994 Wiley-Liss, Inc.

引用

页码：227 / 233

页数：7

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