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Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier.

机译:FISH与染色体特异的端粒探针在相互易位的携带者中快速进行产前诊断。

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Interphase fluorescence in situ hybridization (FISH) analysis has become an accepted practice for rapid preliminary analysis of chromosome aneuploidy from direct amniocyte preparations. The use of dual-color interphase FISH analysis with chromosome-specific protelomere probes for the rapid exclusion of chromosomally unbalanced segregants in the pregnancy of a reciprocal translocation carrier is reported. Amniocentesis was performed at 16 weeks gestation on the carrier of a t(5;14)(p14.2;p13), who was ascertained after the birth of a son with the der(5) chromosome. Interphase FISH analysis with probes for 5pter, 5qter and 14qter showed two signals for each, consistent with alternate segregation of the maternal translocation. Subsequent metaphase analysis confirmed a 46,XY,t(5;14)(p14.2;p13)mat karyotype in the fetus. This case illustrates the utility of interphase FISH analysis with protelomere probes for rapid prenatal diagnosis in cases of parental reciprocal translocation. Copyright 2001 John Wiley & Sons, Ltd.
机译:相间荧光原位杂交(FISH)分析已成为从羊水直接制备中对染色体非整倍性进行快速初步分析的公认方法。据报道,使用双色相间FISH分析与染色体特异的端粒探针可快速排除互易位携带者妊娠中的染色体不平衡分离物。妊娠16周时,对t(5; 14)(p14.2; p13)的携带者进行羊膜穿刺术,该携带者是在生了der(5)染色体的儿子出生后确定的。用5pter,5qter和14qter探针进行的相间FISH分析表明每种信号都有两个信号,这与母体易位的交替分离是一致的。随后的中期分析证实了胎儿的46,XY,t(5; 14)(p14.2; p13)mat核型。该病例说明了在亲本互易的情况下,使用端粒探针进行相间FISH分析对产前快速诊断的实用性。版权所有2001 John Wiley&Sons,Ltd.

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