T(6, 9)(P22.3, Q34) IN A PATIENT WITH REFRACTORY-ANEMIA WITH EXCESS OF BLASTS IN TRANSFORMATION

被引：6

作者：

FERRO, MT ^{[1
]}

RESINO, M ^{[1
]}

CABELLO, P ^{[1
]}

LOPEZYARTO, A ^{[1
]}

MAZARIEGO, YV ^{[1
]}

GARCIASAGREDO, JM ^{[1
]}

STEEGMAN, JL ^{[1
]}

机构：

[1] HOSP PRINCESA,DEPT HEMATOL,MADRID,SPAIN

来源：

CANCER GENETICS AND CYTOGENETICS | 1993年 / 69卷 / 01期

关键词：

D O I：

10.1016/0165-4608(93)90119-7

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

A 40-year-old male was diagnosed with refractory anemia with excess blast in transformation; 11 months later, with the same hematologic situation, a cytogenetic study was carried out on bone marrow and a translocation between chromosomes 6 and 9 with breakpoints at p23 and q34, respectively, was found.

引用

页码：74 / 75

页数：2

共 5 条

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[2] PROGNOSTIC VALUE OF CLONAL CHROMOSOMAL-ABNORMALITIES IN PATIENTS WITH PRIMARY MYELODYSPLASTIC SYNDROMES
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[3] THE SHORT ARM OF CHROMOSOME-6 IS NONRANDOMLY REARRANGED IN SECONDARY MYELODYSPLASTIC SYNDROMES
MECUCCI, C
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[J]. CANCER GENETICS AND CYTOGENETICS, 1988, 31 (02) : 147 - 155
[4] ROWLEY JD, 1976, BLOOD, V47, P705
[5] ACUTE MYELOBLASTIC-LEUKEMIA (AML) WITH T(6-9) (P23-Q34) - A SPECIFIC SUBGROUP OF AML
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[J]. CANCER GENETICS AND CYTOGENETICS, 1983, 10 (02) : 139 - 142

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