PARTIAL TRISOMY-1Q - A NONRANDOM PRIMARY CHROMOSOMAL ABNORMALITY IN MYELODYSPLASTIC SYNDROMES

被引：41

作者：

FONATSCH, C

HAASE, D

FREUND, M

BARTELS, H

TESCH, H

机构：

[1] HANOVER MED SCH,HAMATOL ONKOL ABT,W-3000 HANNOVER 61,GERMANY

[2] UNIV COLOGNE,MED KLIN 1,W-5000 COLOGNE 41,GERMANY

[3] STADT KRANKENHAUS SUD,LUBECK,GERMANY

来源：

CANCER GENETICS AND CYTOGENETICS | 1991年 / 56卷 / 02期

关键词：

D O I：

10.1016/0165-4608(91)90177-V

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Cytogenetic and clinical data of 11 patients with de novo myelodysplastic syndromes and partial or total trisomy of the long arm of chromosome 1 are presented. In eight of these patients trisomy 1q was the sole karyotypic change and therefore can be classified as a primary chromosome anomaly. A remarkably young median age of 36.5 years was noticed in this patient group.

引用

页码：243 / 253

页数：11

共 23 条

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