臂内倒位通常不会产生单着丝粒重组染色体。 - Suppr | 超能文献

Paracentric inversions do not normally generate monocentric recombinant chromosomes.

作者信息

Sutherland G R, Callen D F, Gardner R J

出版信息

Am J Med Genet. 1995 Nov 20;59(3):390-2. doi: 10.1002/ajmg.1320590323.

DOI:10.1002/ajmg.1320590323

Abstract

摘要

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Paracentric inversions do not normally generate monocentric recombinant chromosomes.臂内倒位通常不会产生单着丝粒重组染色体。

Am J Med Genet. 1995 Nov 20;59(3):390-2. doi: 10.1002/ajmg.1320590323.

2

The loss of centromeric heterochromatin from an inactivated centromere of a dicentric chromosome.双着丝粒染色体失活着丝粒的着丝粒异染色质丢失。

Jinrui Idengaku Zasshi. 1986 Mar;31(1):21-6. doi: 10.1007/BF01876798.

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[Pericentric inversion of human chromosomes and its risks] ].[人类染色体的臂间倒位及其风险]

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Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop.重组9号染色体可能源自臂内倒位环中姐妹染色单体的断裂与重连。

Am J Med Genet. 1993 May 15;46(3):304-8. doi: 10.1002/ajmg.1320460313.

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[Paracentric inversions of human chromosomes and their risks].[人类染色体的臂内倒位及其风险]

Cas Lek Cesk. 2004;143(1):35-8.

6

Three large Danish families with a paracentric inversion in the short arm of chromosome N. 5.三个丹麦大家族，其5号染色体短臂存在臂内倒位。

Ann Genet. 1988;31(1):50-2.

7

Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.由母源性臂间倒位内的交叉互换导致的稳定双着丝粒重复-缺失14号染色体

Am J Med Genet. 2002 Dec 15;113(4):333-8. doi: 10.1002/ajmg.b.10720.

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[Chromosome anomalies in 2 cases of human ovarian cancer].

C R Acad Sci III. 1986;302(3):81-6.

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Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH.利用荧光原位杂交技术（FISH）在平衡染色体异常中发现亚端粒区域的意外保留和伴随缺失

Am J Med Genet. 2002 Jul 22;111(1):48-53. doi: 10.1002/ajmg.10535.

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Apparent inverted tandem duplication may result from parental paracentric inversion.明显的倒位串联重复可能源于亲代的臂内倒位。

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Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions.三位臂内倒位杂合男性减数分裂分离模式的断点定位及完整分析。

Eur J Hum Genet. 2009 Jan;17(1):44-50. doi: 10.1038/ejhg.2008.144. Epub 2008 Aug 6.

2

Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions.一个家系中分离出17号染色体短臂臂间倒位时的（17）（p11.2p11.2）缺失的分子分析：对臂间倒位携带者的意义

Am J Hum Genet. 1997 May;60(5):1184-93.