INTERSTITIAL 9Q DELETION - A PRIMARY CHANGE IN A CASE WITH SPLENOMEGALY OF UNKNOWN ORIGIN

被引：0
|
作者：
FERTI, A
TSIKRITZI, H
YIALAMBOUKIDES, M
ECONOMOPOULOS, T
PANANI, A
LYBERATOS, C
机构：
[1] 5th Medical Department, Evangelismos Hospital, Athens
来源：
CANCER GENETICS AND CYTOGENETICS | 1992年 / 58卷 / 02期
关键词：
D O I：
10.1016/0165-4608(92)90114-N
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
In a case with splenomegaly of unknown origin and features of hypersplenism, an interstitial 9q deletion was identified as a sole clonal abnormality of bone marrow cells. The meaning of 9q deletion as a primary change, as well as its clinical significance, are considered.
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页码：201 / 203
页数：3
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