• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Isolation and mapping of a polymorphic DNA sequence (pCMM65) on chromosome 16 [D16S84].

作者信息

Nakamura Y, Martin C, Krapcho K, O'Connell P, Leppert M, Lathrop G M, Lalouel J M, White R

机构信息

Howard Hughes Medical Institute, Salt Lake City, UT 84132.

出版信息

Nucleic Acids Res. 1988 Apr 11;16(7):3122. doi: 10.1093/nar/16.7.3122.

DOI:10.1093/nar/16.7.3122
PMID:2897115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC336475/
Abstract
摘要

相似文献

1
Isolation and mapping of a polymorphic DNA sequence (pCMM65) on chromosome 16 [D16S84].16号染色体[D16S84]上多态性DNA序列（pCMM65）的分离与定位
Nucleic Acids Res. 1988 Apr 11;16(7):3122. doi: 10.1093/nar/16.7.3122.
2
Isolation and mapping of a polymorphic DNA sequence (pB3.811) on chromosome 12 [D12S33].12号染色体上多态性DNA序列（pB3.811）[D12S33]的分离与定位
Nucleic Acids Res. 1989 Jan 25;17(2):823. doi: 10.1093/nar/17.2.823.
3
Isolation and mapping of a polymorphic DNA sequence (cKKA39) on chromosome 14 [D14S23].14号染色体[D14S23]上一个多态性DNA序列（cKKA39）的分离与定位。
Nucleic Acids Res. 1988 Apr 11;16(7):3120. doi: 10.1093/nar/16.7.3120.
4
Isolation and mapping of a polymorphic DNA sequence pYNZ86.1 on chromosome 3 (D3S30).3号染色体（D3S30）上多态性DNA序列pYNZ86.1的分离与定位。
Nucleic Acids Res. 1987 Dec 10;15(23):10079. doi: 10.1093/nar/15.23.10079.
5
Isolation and mapping of a polymorphic DNA sequence pYNM3 on chromosome 8 (D8S38).8号染色体（D8S38）上多态性DNA序列pYNM3的分离与定位。
Nucleic Acids Res. 1987 Dec 10;15(23):10080. doi: 10.1093/nar/15.23.10080.
6
Isolation and mapping of a polymorphic DNA sequence (pEFD53.2) on chromosome 1 [D1S73].1号染色体[D1S73]上一个多态性DNA序列（pEFD53.2）的分离与定位
Nucleic Acids Res. 1988 Apr 11;16(7):3116. doi: 10.1093/nar/16.7.3116.
7
Isolation and mapping of a polymorphic DNA sequence (pTHH55) on chromosome 15 [D15S27].15号染色体[D15S27]上一个多态性DNA序列（pTHH55）的分离与定位。
Nucleic Acids Res. 1988 Apr 11;16(7):3117. doi: 10.1093/nar/16.7.3117.
8
Isolation and mapping of a polymorphic DNA sequence (cMHZ47) on chromosome 13 [D13S52].13号染色体[D13S52]上一个多态性DNA序列（cMHZ47）的分离与定位
Nucleic Acids Res. 1988 Apr 11;16(7):3119. doi: 10.1093/nar/16.7.3119.
9
Isolation and mapping of a polymorphic DNA sequence (pCMM17.1) on chromosome 10 [D10S16].10号染色体上一个多态性DNA序列（pCMM17.1）[D10S16]的分离与定位
Nucleic Acids Res. 1988 Apr 11;16(7):3121. doi: 10.1093/nar/16.7.3121.
10
Isolation and mapping of a polymorphic DNA sequence pEFD122 on chromosome 2 (D2S48).2号染色体（D2S48）上多态性DNA序列pEFD122的分离与定位
Nucleic Acids Res. 1987 Dec 10;15(23):10078. doi: 10.1093/nar/15.23.10078.

引用本文的文献

1
Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression. Absence of linkage to the PKD 1 locus.一个常染色体显性遗传性多囊肾病伴表达降低的大家族的连锁研究。与PKD 1基因座无连锁关系。
Hum Genet. 1990 Jul;85(2):221-7. doi: 10.1007/BF00193200.
2
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.α地中海贫血/智力发育迟缓综合征的临床特征与分子分析。II. α珠蛋白复合体无可检测异常的病例。
Am J Hum Genet. 1990 Jun;46(6):1127-40.
3
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.α地中海贫血/智力发育迟缓综合征的临床特征与分子分析。I. 因涉及染色体带16p13.3的缺失所致病例。
Am J Hum Genet. 1990 Jun;46(6):1112-26.
4
Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16.在16号染色体上鉴定出一个与常染色体显性多囊肾病基因无基因重组的位点。
Am J Hum Genet. 1990 May;46(5):925-33.
5
Organization of variable region segments of the human immunoglobulin heavy chain: duplication of the D5 cluster within the locus and interchromosomal translocation of variable region segments.人类免疫球蛋白重链可变区片段的组织：基因座内D5簇的重复以及可变区片段的染色体间易位。
EMBO J. 1990 Aug;9(8):2501-6. doi: 10.1002/j.1460-2075.1990.tb07429.x.
6
Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.利用基因两侧的多态性DNA标记早期诊断多囊肾病的两步法。
J Med Genet. 1990 Oct;27(10):614-7. doi: 10.1136/jmg.27.10.614.
7
Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).16号染色体短臂上靠近多囊肾病基因（PKD1）的16个多态性位点图谱。
J Med Genet. 1990 Oct;27(10):603-13. doi: 10.1136/jmg.27.10.603.
8
Multipoint mapping of adult onset polycystic kidney disease (PKD1) on chromosome 16.成人多囊肾病（PKD1）在16号染色体上的多点定位。
J Med Genet. 1992 Sep;29(9):638-41. doi: 10.1136/jmg.29.9.638.

本文引用的文献

1
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.人类多位点连锁分析：连锁检测与重组估计
Am J Hum Genet. 1985 May;37(3):482-98.
2
Variable number of tandem repeat (VNTR) markers for human gene mapping.用于人类基因图谱绘制的可变串联重复序列（VNTR）标记
Science. 1987 Mar 27;235(4796):1616-22. doi: 10.1126/science.3029872.