Suppr超能文献

在一群患有畸形和发育迟缓的患者中常规使用提高G带分辨率的方法。

Routine use of methods for improved G-band resolution in a population of patients with malformations and developmental delay.

作者信息

Mascarello J T, Hubbard V

机构信息

Genetic Services, Children's Hospital-San Diego, California 92123.

出版信息

Am J Med Genet. 1991 Jan;38(1):37-42. doi: 10.1002/ajmg.1320380110.

Abstract

We report on an 11-year experience in which cell culture synchronization and other methods for improving cytogenetic detail were used to study 2,245 patients presenting with malformations and (usually) developmental delay. Not including patients presenting with one of the so-called "contiguous gene syndromes," 30 patients (1.1% of the study population) were found to have karyotypes characterized by structural alterations that were either subtle enough to be judged undetectable in standard metaphase preparations or subtle enough to have escaped detection in previous banded studies. Analysis of the detail available for 6 chromosome pairs suggests that the average banding detail available for these analyses fell short of that considered to be "high-resolution" but was, nevertheless, more than would have been expected from standard metaphase preparations.

摘要

我们报告了一项长达11年的研究经历,在此期间,我们运用细胞培养同步化及其他改善细胞遗传学细节的方法,对2245例伴有畸形和(通常)发育迟缓的患者进行了研究。不包括那些患有所谓“连续性基因综合征”的患者,我们发现有30例患者(占研究人群的1.1%)的核型具有结构改变特征,这些改变要么细微到在标准中期制备中被判定无法检测到,要么细微到在之前的显带研究中未被发现。对6对染色体可用细节的分析表明,这些分析可用的平均显带细节未达到被认为是“高分辨率”的水平,但尽管如此,仍比标准中期制备预期的要多。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验