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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。

Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop.

作者信息

Phelan M C, Stevenson R E, Anderson E V

机构信息

Greenwood Genetic Center, SC 29646.

出版信息

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

Abstract

Chromosomally unbalanced offspring resulting from the recombination of parental paracentric inversions are uncommon. We report on a 20-month-old boy with a partial duplication of 9p due to the recombination of a paternal paracentric inversion. The patient's recombinant chromosome was designated rec(9)(p13-->p24::p12-->p24::p12-->qter). The patient's father and paternal aunt have a paracentric inversion of chromosome 9:inv(9)(p13p24). Although several mechanisms have been proposed to explain the chromosome imbalance generated from paracentric inversions, none of the previously described mechanisms can account for the structure of the recombinant chromosome observed in the propositus. We propose an unusual mechanism of formation involving breakage and unequal reunion of sister chromatids within the inversion loop to explain the structure of the patient's recombinant chromosome.

摘要

由亲代臂内倒位重组产生的染色体不平衡后代并不常见。我们报告了一名20个月大的男孩,由于父亲的臂内倒位重组导致9p部分重复。患者的重组染色体被命名为rec(9)(p13→p24::p12→p24::p12→qter)。患者的父亲和姑姑有9号染色体的臂内倒位:inv(9)(p13p24)。尽管已经提出了几种机制来解释由臂内倒位产生的染色体不平衡,但之前描述的任何机制都无法解释先证者中观察到的重组染色体结构。我们提出了一种不寻常的形成机制,涉及倒位环内姐妹染色单体的断裂和不等重聚,以解释患者重组染色体的结构。

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