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Cytogenetic studies in 18 patients with secondary blood disorders.

作者信息

Benitez J, Carbonell F, Ferro T, Prieto F, Sanchez Fayos J

出版信息

Cancer Genet Cytogenet. 1986 Aug;22(4):309-17. doi: 10.1016/0165-4608(86)90023-3.

DOI:10.1016/0165-4608(86)90023-3
PMID:3460686
Abstract

Cytogenetic studies were carried out in 18 patients with secondary blood diseases; 15 patients had a history of prior malignancy, two had been professionally exposed to carcinogenic agents, and one patient had been treated with immunodepressors. The interval between initial therapy and secondary disease ranged from 13 to 123 months, with a mean of 57.8 months; the mean survival time from the diagnosis of secondary disease was 6 months. Cytogenetic abnormalities were present in 83% of cases, with a trend to hypodiploidy in 90%. The most often involved chromosomes were #5, #7, and 3p. A correlation between the cytogenetic abnormalities and etiologic factors has been analyzed; data from the present series and from the literature suggest a correlation between chromosome #7 and chemical agents, and chromosomes #11, #12, and #17 and physical agents.

摘要

相似文献

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引用本文的文献

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Genetic markers on chromosome 7.7号染色体上的遗传标记。
J Med Genet. 1988 May;25(5):294-306. doi: 10.1136/jmg.25.5.294.
2
Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene.用于克隆囊性纤维化基因的7号染色体上DNA标记的鉴定及区域定位。
Am J Hum Genet. 1988 Nov;43(5):645-63.
3
Transforming genes and chromosome aberrations in therapy-related leukemia and myelodysplastic syndrome.
Ann Hematol. 1991 Jun;62(6):211-6. doi: 10.1007/BF01729834.