A simple non-radioactive method for diagnosis of Huntington's disease.

作者信息

Valdes J M, Tagle D A, Elmer L W, Collins F S

机构信息

Cellular and Molecular Biology Program, University of Michigan, Ann Arbor 48109-0650.

出版信息

Hum Mol Genet. 1993 Jun;2(6):633-4. doi: 10.1093/hmg/2.6.633.

DOI:10.1093/hmg/2.6.633

PMID:8353481

Abstract

摘要

相似文献

A simple non-radioactive method for diagnosis of Huntington's disease.

Hum Mol Genet. 1993 Jun;2(6):633-4. doi: 10.1093/hmg/2.6.633.

Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease.

Hum Mol Genet. 1993 Jun;2(6):637. doi: 10.1093/hmg/2.6.637.

Improving diagnosis of Huntington's disease by analysis of an intragenic trinucleotide repeat expansion.

Med J Aust. 1995 Apr 3;162(7):385, 387. doi: 10.5694/j.1326-5377.1995.tb139951.x.

A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes.

Mol Cell Probes. 1993 Jun;7(3):235-9. doi: 10.1006/mcpr.1993.1034.

A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease.

Hum Mol Genet. 1993 Jun;2(6):635-6. doi: 10.1093/hmg/2.6.635.

[Gene identification for Huntington's disease. Direkt mutational analysis confirms the diagnosis].

Lakartidningen. 1995 Jan 4;92(1-2):28-31.

Fluorescence PCR and GeneScan analysis for the detection of CAG repeat expansions associated with Huntington's disease.

Methods Mol Biol. 2003;217:101-8. doi: 10.1385/1-59259-330-5:101.

Borderline repeat expansion in Huntington's disease.

Lancet. 1993 Dec 11;342(8885):1491-2. doi: 10.1016/0140-6736(93)92974-x.

Molecular analysis of the Huntington's disease gene in New Zealand.

N Z Med J. 1996 Feb 9;109(1015):27-30.

[Pre-symptomatic diagnosis of Huntington disease by polymerase chain reaction].

Orv Hetil. 1996 Mar 3;137(9):451-4.

引用本文的文献

The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size.

Am J Hum Genet. 1997 May;60(5):1202-10.

The gene for Huntington's disease.

BMJ. 1993 Aug 14;307(6901):396-7. doi: 10.1136/bmj.307.6901.396.

Island rescue PCR: a rapid and efficient method for isolating transcribed sequences from yeast artificial chromosomes and cosmids.

Proc Natl Acad Sci U S A. 1994 Jun 7;91(12):5377-81. doi: 10.1073/pnas.91.12.5377.

A specific mutation for Huntington's disease.

J Med Genet. 1993 Dec;30(12):975-7. doi: 10.1136/jmg.30.12.975.

A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.

J Med Genet. 1993 Dec;30(12):1003-7. doi: 10.1136/jmg.30.12.1003.

Trinucleotide (CAG) repeat expansion in chromosomes of Spanish patients with Huntington's disease.

Hum Genet. 1994 Nov;94(5):563-4. doi: 10.1007/BF00211028.

Chemiluminescent detection of blotted PCR products (CB-PCR) of two CAG dynamic mutations (Huntington's disease and spinocerebellar ataxia type 1).

J Med Genet. 1994 Aug;31(8):654-5. doi: 10.1136/jmg.31.8.654.

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