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对涉及6号、12号、14号和16号染色体上9个断点的复杂染色体重排进行荧光原位杂交(FISH)分析。

FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16.

作者信息

Phelan M C, Blackburn W, Rogers R C, Crawford E C, Cooley N R, Schrock E, Ning Y, Ried T

机构信息

Greenwood Genetic Center, Greenwood, SC 29646, USA.

出版信息

Prenat Diagn. 1998 Nov;18(11):1174-80.

PMID:9854728
Abstract

We report the prenatal diagnosis of an apparently balanced de novo complex chromosome rearrangement (CCR) which involved nine breakpoints on four different chromosomes. Fluorescence in situ hybridization (FISH) and spectral karyotyping (SKY) were performed as an adjunct to G-banding for characterization of the abnormal chromosomes. The 22-week female fetus showed minor dysmorphic features including dolichocephaly, broad fingernails, tibial bowing, clubfoot, thoracolumbar scoliosis and hypoplastic toenails. Autopsy revealed gall-bladder hypoplasia and an atrial septal defect. Chromosome analysis of fetal tissue confirmed the presence of the complex rearrangement.

摘要

我们报告了一例产前诊断的明显平衡的新发复杂染色体重排(CCR),该重排涉及四条不同染色体上的九个断点。荧光原位杂交(FISH)和光谱核型分析(SKY)作为G显带的辅助手段用于异常染色体的特征分析。这名22周大的女胎表现出一些轻微的畸形特征,包括长头畸形、指甲宽大、胫骨弯曲、马蹄内翻足、胸腰椎脊柱侧弯和趾甲发育不全。尸检发现胆囊发育不全和房间隔缺损。胎儿组织的染色体分析证实了复杂重排的存在。

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