Suppr超能文献

前脑无裂畸形合并7号染色体长臂结构重排患者的分子细胞遗传学分析

Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q.

作者信息

Vance G H, Nickerson C, Sarnat L, Zhang A, Henegariu O, Morichon-Delvallez N, Butler M G, Palmer C G

机构信息

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis 46202-5251, USA.

出版信息

Am J Med Genet. 1998 Feb 26;76(1):51-7.

Abstract

The holoprosencephaly (HPE) sequence is a malformation complex with abnormal midline cleavage of the embryonic forebrain. HPE is genetically heterogeneous with at least 6 different chromosome regions containing genes involved in the expression of the phenotype. HPE3, recently identified as the human Sonic hedgehog gene, is localized to 7q36. We have used fluorescence in situ hybridization (FISH) and polymerase chain reaction (PCR) amplification in 5 cell lines from patients with HPE (3 cases), HPE and sacral agenesis (1 case), and microcephaly (1 case) to further define the structural rearrangements of the long arm of chromosome 7 in each case. All cell lines demonstrated loss of material in the critical region of HPE3 at band 7q36, which includes the Sonic hedgehog gene. We report here the analysis of these patient cell lines.

摘要

前脑无裂畸形(HPE)序列是一种伴有胚胎前脑中线分裂异常的畸形综合征。HPE具有遗传异质性,至少有6个不同的染色体区域包含与该表型表达相关的基因。最近被鉴定为人类音猬因子基因的HPE3定位于7q36。我们运用荧光原位杂交(FISH)和聚合酶链反应(PCR)扩增技术,对来自患有HPE(3例)、HPE合并骶骨发育不全(1例)以及小头畸形(1例)患者的5个细胞系进行检测,以进一步明确每种情况下7号染色体长臂的结构重排。所有细胞系均显示在7q36带的HPE3关键区域存在物质缺失,该区域包含音猬因子基因。我们在此报告对这些患者细胞系的分析结果。

相似文献

4
De novo 7q36 deletion: breakpoint analysis and types of holoprosencephaly.新发7q36缺失:断点分析与全前脑畸形类型
Am J Med Genet. 1998 Jan 13;75(2):153-8. doi: 10.1002/(sici)1096-8628(19980113)75:2<153::aid-ajmg6>3.0.co;2-u.

本文引用的文献

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