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运用针对小标记染色体进行细胞遗传学分型的合理策略,通过染色体特异性DNA探针鉴定出一条额外的der(18)染色体。

Identification of a supernumerary der(18) chromosome by a rational strategy for the cytogenetic typing of small marker chromosomes with chromosome-specific DNA probes.

作者信息

Koch J, Fischer H, Askholm H, Hindkjaer J, Pedersen S, Kølvraa S, Bolund L

机构信息

Institute of Human Genetics, University of Aarhus, Denmark.

出版信息

Clin Genet. 1993 Apr;43(4):200-3. doi: 10.1111/j.1399-0004.1993.tb04448.x.

Abstract

A case of a supernumerary der(18) marker chromosome is presented. The chromosomal origin of the marker chromosome was not evident by traditional chromosome analysis, but was determined by PRimed IN Situ labelling (PRINS) with chromosome specific centromere probes as primers for chain elongation in situ. For this purpose a strategy was developed which, in a few simple reactions, makes it possible unequivocally to determine the origin of any small marker chromosome. The approach does not require any hints about the origin of the chromosome prior to the analysis, since the chromosomal origin of the marker is established through PRINS reactions with pooled and single chromosome-specific centromere probes. Identification, mosaic screening and structural analysis require a total of 8-9 such reactions and may, due to the extreme speed of the PRINS reaction, be obtained within a single working day.

摘要

本文报道了一例额外的der(18)标记染色体病例。通过传统染色体分析,标记染色体的染色体起源并不明显,但通过以染色体特异性着丝粒探针作为原位链延伸引物的引物原位标记(PRINS)得以确定。为此开发了一种策略,通过几个简单反应就能够明确确定任何小标记染色体的起源。该方法在分析前不需要关于染色体起源的任何提示,因为标记染色体的染色体起源是通过与混合及单一染色体特异性着丝粒探针的PRINS反应来确定的。鉴定、嵌合体筛查和结构分析总共需要8 - 9个这样的反应,并且由于PRINS反应速度极快,可能在单个工作日内完成。

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