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胰蛋白酶显带的人类近端着丝粒染色体的非随机关联。

Non-random association of trypsin-banded human acrocentric chromosomes.

作者信息

Galperin-Lemaître H, Hens L, Kirsch-Volders M, Susanne C

出版信息

Hum Genet. 1977 Mar 14;35(3):261-8. doi: 10.1007/BF00446619.

Abstract

This paper deals with a computer-aided study of the associations between acrocentric chromosomes as well as between those other chromosomes which in our investigations were revealed to be significantly closer to each other than random. The chromosome pairs were identified by a trypsin-banding technique. The method used has been elaborated previously with the specific aim of determining associations in a manner that avoids all subjective criteria. The tendency for association between homologous chromosomes is in decreasing order: 21 and 13 greater than 1 greater than 14, 18 and 19 greater than 17. Among the nonhomologous acrocentric chromosomes the significant tendencies for associations are between D-D: 13-14 greater than 13-15 greater than 14-15; between D-G: 13-21 greater than 14-21 greater than 13-22 greater than 15-22. The implication of the different tendencies to associate are dicussed in terms of aetiology of numerical and structural chromosome abnormalities.

摘要

本文探讨了对近端着丝粒染色体之间以及在我们的研究中发现彼此之间比随机情况显著更接近的其他染色体之间的关联进行计算机辅助研究。染色体对通过胰蛋白酶显带技术进行识别。之前已经详细阐述了所使用的方法,其特定目的是以避免所有主观标准的方式确定关联。同源染色体之间的关联倾向按降序排列为:21号和13号染色体大于1号染色体大于14号、18号和19号染色体大于17号染色体。在非同源近端着丝粒染色体中,显著的关联倾向存在于D-D染色体之间:13-14大于13-15大于14-15;在D-G染色体之间:13-21大于14-21大于13-22大于15-22。从染色体数目和结构异常的病因学角度讨论了不同关联倾向的意义。

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