7号染色体上的遗传标记。
Genetic markers on chromosome 7.
作者信息
Tsui L C
机构信息
Department of Genetics, Hospital for Sick Children, Toronto, Ontario, Canada.
出版信息
J Med Genet. 1988 May;25(5):294-306. doi: 10.1136/jmg.25.5.294.
Abstract
Chromosome 7 is frequently associated with chromosome aberrations, rearrangements, and deletions. It also contains many important genes, gene families, and disease loci. This brief review attempts to summarise these and other interesting aspects of chromosome 7. With the rapid accumulation of cloned genes and polymorphic DNA fragments, this chromosome has become an excellent substrate for molecular genetic studies.
摘要
7号染色体常与染色体畸变、重排及缺失相关。它还包含许多重要基因、基因家族及疾病位点。本简要综述试图总结7号染色体的这些及其他有趣方面。随着克隆基因和多态性DNA片段的迅速积累，这条染色体已成为分子遗传学研究的优良对象。
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本文引用的文献
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The mapping of human chromosomes.人类染色体的图谱绘制。
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Chromosome 7 in ataxia-telangiectasia.共济失调毛细血管扩张症中的7号染色体。
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Interstitial deletion of the long arm of chromosome 7.7号染色体长臂的间质缺失。
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High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia.共济失调毛细血管扩张症中7号和14号染色体的倒位和易位频率较高。
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Chromosome pattern, occupation, and clinical features in patients with acute nonlymphocytic leukemia.急性非淋巴细胞白血病患者的染色体模式、职业及临床特征
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Interstitial deletion of the short arm of chromosome 7 without craniosynostosis.7号染色体短臂间质性缺失，无颅缝早闭。
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The pattern of radiation-induced transmissible aberrations in a human cell culture.人类细胞培养中辐射诱导的可传递畸变模式。
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