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Tandem duplication q14 and dicentric formation by end-to-end chromosome fusions in ataxia telandiectasia (AT). Clinical and cytogenetic findings in 5 patients.

作者信息

Hayashi K, Schmid W

出版信息

Humangenetik. 1975 Nov 6;30(2):135-41. doi: 10.1007/BF00291946.

DOI:10.1007/BF00291946
PMID:1193600
Abstract

Chromosome studies on lymphocyte cultures were performed in 5 patients with AT, 2 of whom had been followed for 4 years. Four out of these patients showed an increased incidence of chromosome-type aberrations. A clonal development was present in one patient, 96% of his metaphases containing a tandem duplication of almost the entire long arm 14. Four years earlier the proportion of these cells was 80%. Two other patients presented a small proportion of cells with an unidentified abnormally long D chromosome. In a total of 724 metaphases from 4 patients 31 dicentric chromosomes were observed, all of a peculiar type; in their formation no chromosome material was lost and they all seem to have arisen by end-to-end fusions. The incidence of chromatid-type aberrations was normal or at the upper limit of control values in all 5 cases. The sister chromatid exchange rate studied with BUDR in 3 patients was found to be normal.

摘要

相似文献

1
Tandem duplication q14 and dicentric formation by end-to-end chromosome fusions in ataxia telandiectasia (AT). Clinical and cytogenetic findings in 5 patients.
Humangenetik. 1975 Nov 6;30(2):135-41. doi: 10.1007/BF00291946.
2
Cytogenetic study of patients with ataxia-telangiectasia.
Humangenetik. 1974;24(2):115-28. doi: 10.1007/BF00283768.
3
Specific chromosome aberrations in ataxia telangiectasia.共济失调毛细血管扩张症中的特定染色体畸变。
J Med Genet. 1975 Sep;12(3):251-62. doi: 10.1136/jmg.12.3.251.
4
Apparent "in situ" clone of cytogenetically marked ataxia-telangiectasia lymphocytes.细胞遗传学标记的共济失调毛细血管扩张症淋巴细胞的明显“原位”克隆。
Humangenetik. 1975 Sep 20;30(3):251-7. doi: 10.1007/BF00279190.
5
A 14/14 marker chromosome lymphocyte clone in ataxia telangiectasia.共济失调毛细血管扩张症中的一个具有14/14标记染色体的淋巴细胞克隆。
J Hered. 1975 Jan-Feb;66(1):33-5. doi: 10.1093/oxfordjournals.jhered.a108569.
6
Evolution of chromosomal abnormalities in sequential cytogenetic studies of ataxia telangiectasia.共济失调毛细血管扩张症连续细胞遗传学研究中染色体异常的演变
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7
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8
Unrepaired DNA strand breaks in irradiated ataxia telangiectasia lymphocytes suggested from cytogenetic observations.细胞遗传学观察提示,共济失调毛细血管扩张症淋巴细胞经照射后存在未修复的DNA链断裂。
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9
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10
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Mutat Res. 1995 Feb;334(1):59-69. doi: 10.1016/0165-1161(95)90031-4.

引用本文的文献

1
Telomeric Associations.端粒关联
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2
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Hum Genet. 1980;54(1):69-77. doi: 10.1007/BF00279051.
3
Genetic and cytological characterisation of fusion chromosomes of Dictyostelium discoideum.盘基网柄菌融合染色体的遗传与细胞学特征分析

本文引用的文献

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Ataxia-telangiectasia. A report of two cases in siblings presenting a picture of progressive spinal muscular atrophy.
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Chromosomal abnormalities in ataxia-telangiectasia (Louis Bar's syndrome).共济失调毛细血管扩张症(路易斯·巴尔综合征)中的染色体异常。
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Cytogenetic findings in two brothers with ataxia-telangiectasia (Louis Bar's syndrome).两例共济失调毛细血管扩张症(路易斯·巴尔综合征)患者兄弟的细胞遗传学研究结果
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Tandem translocation t(14;14) in isolated and clonal cells in ataxia telangiectasia are different.共济失调毛细血管扩张症中分离的克隆细胞中的串联易位t(14;14)有所不同。
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Telomere association of chromosomes induced by aphidicolin in a normal individual.
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Ataxia-telangiectasia--clonal growth of translocation lymphocytes.共济失调毛细血管扩张症——易位淋巴细胞的克隆性生长。
N Engl J Med. 1973 Aug 9;289(6):286-91. doi: 10.1056/NEJM197308092890603.
5
Cytogenetic study of patients with ataxia-telangiectasia.
Humangenetik. 1974;24(2):115-28. doi: 10.1007/BF00283768.
6
A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes.布卢姆综合征淋巴细胞中姐妹染色单体交换的多重增加。
Proc Natl Acad Sci U S A. 1974 Nov;71(11):4508-12. doi: 10.1073/pnas.71.11.4508.
7
A rapid banding technique for human chromosomes.一种用于人类染色体的快速显带技术。
Lancet. 1971 Oct 30;2(7731):971-2. doi: 10.1016/s0140-6736(71)90287-x.
8
The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts.在范科尼贫血中,姐妹染色单体交换率与自发染色体断裂平行,在人类淋巴细胞和成纤维细胞中与三胺硫磷诱导的畸变平行。
Humangenetik. 1975 Sep 23;29(3):201-6. doi: 10.1007/BF00297624.