Suppr超能文献

18号染色体臂间倒位携带者的两名后代出现18号染色体部分单体和部分三体。

Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18.

作者信息

Vianna-Morgante A M, Nozaki M J, Ortega C C, Coates V, Yamamura Y

出版信息

J Med Genet. 1976 Oct;13(5):366-70. doi: 10.1136/jmg.13.5.366.

Abstract

A pericentric inversion of chromosome 18 is described in the mother of a patient with clinical diagnosis of 18q--syndrome. The propositus' chromosome complement includes the recombinant 18 with deficiency of the distal one-third of the long arm and duplication of the terminal segment of the short arm. The propositus' sister carrier the recombinant 18 with a duplication of the distal one-third of the long arm and a deficiency of the terminal segment of the short arm. The relative length of the inverted segment represents about 60% of the total chromosome 18 length. The probability of recombinant formation following the occurrence of a chiasma within the inverted segment is predicted to be high.

摘要

在一名临床诊断为18q-综合征患者的母亲中发现了18号染色体的臂间倒位。先证者的染色体组成包括重组的18号染色体,其长臂远端三分之一缺失,短臂末端片段重复。先证者的姐姐携带重组的18号染色体,其长臂远端三分之一重复,短臂末端片段缺失。倒位片段的相对长度约占18号染色体全长的60%。预计在倒位片段内出现交叉后形成重组体的概率很高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3358/1013442/41b4b4bfbd0c/jmedgene00312-0031-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验