ABNORMALITIES OF CHROMOSOME-18 IN MYELODYSPLASTIC SYNDROMES AND SECONDARY LEUKEMIA

被引：7

作者：

BERGER, R ^{[1
]}

LECONIAT, M ^{[1
]}

DERRE, J ^{[1
]}

FLEXOR, MA ^{[1
]}

HILLION, J ^{[1
]}

机构：

[1] INST GENET MOLEC,CNRS,SDI 15954I,PARIS,FRANCE

来源：

CANCER GENETICS AND CYTOGENETICS | 1992年 / 63卷 / 02期

关键词：

D O I：

10.1016/0165-4608(92)90387-N

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Monosomy 18 and partial deletion of 18q are nonrandom events in myelodysplastic syndromes (MDS) and secondary acute myeloblastic leukemia (sAML). They are part of complex chromosome abnormalities, as shown in the present study of six patients with MDS and sAML. We compared occurrence of chromosome 18 abnormalities in these syndromes with that in de novo AML.

引用

页码：97 / 99

页数：3

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