Suppr超能文献

由于一个inv ins(7;2)(q21.2;q3105q24.2)在四代人中分离,导致纯合的2q24.2----q3105单体和三体。

Pure monosomy and trisomy 2q24.2----q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generations.

作者信息

Moller M, García-Cruz D, Rivera H, Sánchez-Corona J, Cantú J M

出版信息

Hum Genet. 1984;68(1):77-86. doi: 10.1007/BF00293878.

Abstract

An inv ins(7;2)(q21.2;q3105q24.2) was found to segregate through four generations of a family. Adjacent-1 segregation aneusomies were ascertained in five patients: three monosomics and two trisomics; and the corresponding syndromes were delineated. The comparative analysis between these and other previously described 2q aneusomic individuals led to the conclusion that a large cleft between first and second toes is a constant feature in monosomy 2q24----q31. No other trait could plausibly be mapped. Risks of 7.9 to 31.6% for aneusomic children and of 26.3% for abortion were estimated in the present family.

摘要

在一个家族的四代人中发现了inv ins(7;2)(q21.2;q3105q24.2)。在5名患者中确定了邻接-1分离非整倍体:3名单体和2名三体;并描述了相应的综合征。对这些患者与其他先前描述的2q非整倍体个体进行比较分析后得出结论,2q24----q31单体中第一和第二脚趾之间的大裂缺是一个恒定特征。没有其他特征可以合理定位。在当前家族中,非整倍体儿童的风险估计为7.9%至31.6%,流产风险为26.3%。

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