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Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity.

作者信息

Sharp C B, Bedford H M, Willard H F

机构信息

Department of Medical Genetics, University of Toronto, Ontario, Canada.

出版信息

Hum Genet. 1990 Aug;85(3):330-6. doi: 10.1007/BF00206757.

DOI:10.1007/BF00206757
PMID:2394446
Abstract

Three different long-arm X isochromosomes and an isodicentric X chromosome were examined by in situ hybridization with X-chromosome-specific alpha-satellite probes and by quantitation of Southern blots hybridized with proximal short-arm probes. Each chromosome had a unique pericentromeric structure. The isodicentric X chromosome was clearly dicentric, showing two distinct alpha-satellite hybridization signals and duplication of short-arm material. Two isochromosomes showed a larger than normal, bifid alpha-satellite signal and also had duplications of different extents of short-arm material. The third X isochromosome could not be distinguished from a classical long-arm isochromosome; it did not have a short-arm duplication and it had a single alpha-satellite signal. These data indicate that rearrangements responsible for X isochromosome formation can occur at numerous locations in the pericentromeric region and that some X isochromosomes may involve duplications of substantial portions of the short arm.

摘要

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本文引用的文献

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The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism.与特纳综合征相关的染色体基因型分布:活产患病率以及与结构性X异常或嵌合体相关的基因型中胎儿死亡率降低和严重程度减轻的证据。
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来自失活X染色体的基因表达异质性:一个X连锁基因,在某些人类细胞系中逃脱了X染色体失活,但在其他细胞系中则被失活。
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Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.与人类X染色体等臂染色体相关的断点的分子定义:对形成机制的启示
Am J Hum Genet. 1996 Jan;58(1):154-60.
6
A stable dicentric chromosome: both centromeres develop kinetochores and attach to the spindle in monocentric and dicentric configuration.一条稳定的双着丝粒染色体:两个着丝粒都形成动粒,并以单着丝粒和双着丝粒构型附着于纺锤体。
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Cytogenet Cell Genet. 1973;12(5):372-3. doi: 10.1159/000130478.
5
Cytogenetic findings in 89 cases of Turner's syndrome with abnormal karyotypes.89例核型异常的特纳综合征的细胞遗传学研究结果
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Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences.利用DNA序列多态性确定人类X等臂染色体的起源并检测一条带有Xp序列的明显i(Xq)。
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8
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.使用定量、高灵敏度荧光杂交技术的细胞遗传学分析。
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Dicentric chromosomes and the inactivation of the centromere.双着丝粒染色体与着丝粒失活
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