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centromere misdivision
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  “centromere misdivision”译为未确定词的双语例句
     The del(X) (p11) occurred through X chromosome breakage and deletion machanism. The i(Xq) resulted from X chromosome centromere misdivision in oocyte.
     dup(X)(p21)是由X染色体姊妹染色单体不均等的互换所引起的,del(X)(p11)是由于X染色体断裂后丢失所致,i(Xq)的发生是由于卵母细胞X染色体着丝粒错分裂。
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  相似匹配句对
     The del(X) (p11) occurred through X chromosome breakage and deletion machanism. The i(Xq) resulted from X chromosome centromere misdivision in oocyte.
     dup(X)(p21)是由X染色体姊妹染色单体不均等的互换所引起的,del(X)(p11)是由于X染色体断裂后丢失所致,i(Xq)的发生是由于卵母细胞X染色体着丝粒错分裂。
短句来源
     AUTOMATIC SEEKING OF CHROMOSOME CENTROMERE
     怎样自动寻找染色体的着丝粒
短句来源
     THE DETECTION OF CENTROMERE PROTEINS IN Tetrahmena thermophila
     嗜热四膜虫的着丝粒蛋白检查
短句来源
     2. One-time misdivision event including two chromotids.
     2、一次包括两条染色单体的错分裂.
短句来源
     3. Two-time misdivision event including two chromotids.
     3、二次包括两条染色单体的错分裂.
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  centromere misdivision
The Iso-B was derived from the Deficient by centromere misdivision, the long arm forming the Iso-B.
      
The most frequently observed B mutation was centromere misdivision with chromatid nondisjunction giving rise to iso-B-chromosomes.
      
The breakpoints of five B centromere misdivision derivatives are mapped within this domain.
      
The Pedigree and Structure of the B Centromere Misdivision Derivatives.
      
Successive rounds of centromere misdivision are used to whittle down the maize B chromosome centromere region from 9 Mbp to less than 1 Mbp.
      
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In this study, we analysed the parental origin and mechanism of X chromosome abnorma-lites in 3 cases by using RFLPs on short or long arm of X chromosome as genetic markers. Their karyotypes were 46,X,dup(X)(p21); 46,X,del(X)(p11); 46,X,i(Xq). The results demonstrated that the dup(X)(p21) and the del(X)(pll) were of paternal origin and i(Xq) was of maternal origin. The dup(X)(p21) arose from an unequal sister chromatid exchange. The del(X) (p11) occurred through X chromosome breakage and deletion machanism....

In this study, we analysed the parental origin and mechanism of X chromosome abnorma-lites in 3 cases by using RFLPs on short or long arm of X chromosome as genetic markers. Their karyotypes were 46,X,dup(X)(p21); 46,X,del(X)(p11); 46,X,i(Xq). The results demonstrated that the dup(X)(p21) and the del(X)(pll) were of paternal origin and i(Xq) was of maternal origin. The dup(X)(p21) arose from an unequal sister chromatid exchange. The del(X) (p11) occurred through X chromosome breakage and deletion machanism. The i(Xq) resulted from X chromosome centromere misdivision in oocyte.

本文对三例X染色体结构异常46,X,dup(X)(p21);46,X,del(X)(p11);46,X,i(Xq)患者及其父母,用X染色体短臂或长臂上的限制性片段长度多态性(RFLPs)作为遗传标记,研究了异常X染色体的起源和形成机理。结果表明,dup(X)(p21)和del(X)(p11)起源于父方,而i(Xq)起源于母方。dup(X)(p21)是由X染色体姊妹染色单体不均等的互换所引起的,del(X)(p11)是由于X染色体断裂后丢失所致,i(Xq)的发生是由于卵母细胞X染色体着丝粒错分裂。

 
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