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原位杂交与易位断点图谱分析。III. 伴有22号染色体部分单体性的迪格奥尔格综合征

In situ hybridization and translocation breakpoint mapping. III. DiGeorge syndrome with partial monosomy of chromosome 22.

作者信息

Cannizzaro L A, Emanuel B S

出版信息

Cytogenet Cell Genet. 1985;39(3):179-83. doi: 10.1159/000132131.

Abstract

We have performed in situ hybridization of a probe for the lambda IGLC constant region to metaphase spreads from two DiGeorge syndrome (DGS)-related chromosomal rearrangements with breakpoints in 22q11. In this study we have demonstrated that the breakpoints are proximal to the lambda IGLC constant region cluster. Thus, at the molecular level, DGS-related breakpoints can be distinguished from the 22q11 breakpoint of CML, but not from the 8;22 translocation of Burkitt lymphoma or from the 21;22 translocations that we have previously studied.

摘要

我们用一个针对λ免疫球蛋白轻链恒定区的探针,对来自两个与迪乔治综合征(DGS)相关的染色体重排的中期染色体铺展进行了原位杂交,这两个染色体重排在22q11处有断点。在本研究中,我们证明这些断点位于λ免疫球蛋白轻链恒定区簇的近端。因此,在分子水平上,与DGS相关的断点可与慢性粒细胞白血病(CML)的22q11断点区分开来,但无法与伯基特淋巴瘤的8;22易位或我们之前研究过的21;22易位区分开来。

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