D11S35位点的二核苷酸重复多态性 - Suppr

Suppr

超能文献

Dinucleotide repeat polymorphism at the D11S35 locus.

作者信息

Litt M, Sharma V, Luty J A

机构信息

Oregon Health Sciences University, Portland 97201.

出版信息

Nucleic Acids Res. 1990 Oct 11;18(19):5921. doi: 10.1093/nar/18.19.5921-a.

DOI:10.1093/nar/18.19.5921-a

PMID:2216804

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC332371/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6660/332371/2007d22d72dd/nar00203-0304-a.jpg

相似文献

Dinucleotide repeat polymorphism at the D11S35 locus.D11S35位点的二核苷酸重复多态性

Nucleic Acids Res. 1990 Oct 11;18(19):5921. doi: 10.1093/nar/18.19.5921-a.

Dinucleotide repeat polymorphism at the D11S420 locus.D11S420位点的二核苷酸重复多态性。

Nucleic Acids Res. 1990 Oct 11;18(19):5920. doi: 10.1093/nar/18.19.5920.

Dinucleotide repeat polymorphism at the D11S490 locus.位于D11S490位点的二核苷酸重复多态性

Nucleic Acids Res. 1990 Dec 25;18(24):7470. doi: 10.1093/nar/18.24.7470.

Dinucleotide repeat polymorphism at the D11S528 locus.D11S528基因座的二核苷酸重复多态性

Nucleic Acids Res. 1991 Apr 25;19(8):1964. doi: 10.1093/nar/19.8.1964.

Dinucleotide repeat polymorphism at the D11S436 locus.D11S436位点的二核苷酸重复多态性。

Nucleic Acids Res. 1991 Dec 25;19(24):6981. doi: 10.1093/nar/19.24.6981.

Dinucleotide repeat polymorphism at the D11S860 locus.D11S860位点的二核苷酸重复多态性

Nucleic Acids Res. 1992 Mar 11;20(5):1161. doi: 10.1093/nar/20.5.1161-a.

Dinucleotide repeat polymorphism at the D11S527 locus.D11S527位点的二核苷酸重复多态性

Nucleic Acids Res. 1991 Sep 11;19(17):4790. doi: 10.1093/nar/19.17.4790-a.

Dinucleotide repeat polymorphism at D11S994 locus.

Hum Mol Genet. 1993 Oct;2(10):1747. doi: 10.1093/hmg/2.10.1747.

Highly informative dinucleotide repeat polymorphism at the D11S29 locus on chromosome 11q23.位于11号染色体11q23区域的D11S29位点存在高信息量的二核苷酸重复多态性。

Hum Genet. 1992 May;89(3):357-9. doi: 10.1007/BF00220560.

Dinucleotide repeat polymorphism at the int-2 proto-oncogene locus (INT2).原癌基因int-2位点（INT2）的二核苷酸重复多态性

Nucleic Acids Res. 1990 Dec 25;18(24):7468.

引用本文的文献

Linkage analysis in Usher syndrome type I (USH1) families from Spain.对来自西班牙的Ⅰ型Usher综合征（USH1）家族进行连锁分析。

J Med Genet. 1998 May;35(5):391-8. doi: 10.1136/jmg.35.5.391.

Genetic linkage analysis of 14 candidate gene loci in a family with autosomal dominant osteoarthritis without dysplasia.对一个无发育异常的常染色体显性骨关节炎家族中的14个候选基因位点进行基因连锁分析。

J Med Genet. 1997 Dec;34(12):1024-7. doi: 10.1136/jmg.34.12.1024.

Genetic variation of microsatellite markers D1S117, D6S89, D11S35, APOC2, and D21S168 in the Spanish population.西班牙人群中微卫星标记D1S117、D6S89、D11S35、载脂蛋白C2（APOC2）和D21S168的基因变异

Int J Legal Med. 1993;105(5):271-7. doi: 10.1007/BF01370384.

Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q.对另一个患有遗传性非嗜铬性副神经节瘤的家族进行分析后，发现潜在基因位于11号染色体q臂近端区域。

Hum Genet. 1993 May;91(4):357-61. doi: 10.1007/BF00217356.

Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.精神分裂症相关的11号染色体q21易位：侧翼标记的鉴定以及11号染色体q片段杂种的构建作为克隆和定位资源

Am J Hum Genet. 1993 Mar;52(3):478-90.

Absence of linkage to the ataxia telangiectasia locus in familial breast cancer.

Hum Genet. 1993 Aug;92(1):91-4. doi: 10.1007/BF00216153.

Loss of heterozygosity in cervical carcinoma: subchromosomal localization of a putative tumor-suppressor gene to chromosome 11q22-q24.宫颈癌中的杂合性缺失：一个假定的肿瘤抑制基因在染色体11q22 - q24上的亚染色体定位

Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):6953-7. doi: 10.1073/pnas.91.15.6953.

Loss of heterozygosity at chromosome 11 in breast cancer: association of prognostic factors with genetic alterations.乳腺癌11号染色体杂合性缺失：预后因素与基因改变的关联

Br J Cancer. 1995 Sep;72(3):696-701. doi: 10.1038/bjc.1995.396.

Localization of an ataxia-telangiectasia gene to an approximately 500-kb interval on chromosome 11q23.1: linkage analysis of 176 families by an international consortium.共济失调毛细血管扩张症基因定位于11号染色体q23.1上一个约500千碱基对的区间：一个国际联盟对176个家族进行的连锁分析

Am J Hum Genet. 1995 Jul;57(1):112-9.

Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinism.一名患有酪氨酸酶阴性（IA型）眼皮肤白化病的美国黑人中酪氨酸酶基因突变纯合子。

Am J Hum Genet. 1991 Feb;48(2):318-24.

本文引用的文献

Seven polymorphic loci mapping to human chromosomal region 11q22-qter.七个多态性位点定位于人类染色体区域11q22 - qter。

Genomics. 1988 Jan;2(1):66-75. doi: 10.1016/0888-7543(88)90110-3.

A detailed genetic map of the long arm of chromosome 11.

Genomics. 1990 Jul;7(3):335-45. doi: 10.1016/0888-7543(90)90167-s.

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