• 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

相似文献

1
DGGE detection of HhaI polymorphism in the F9 gene.F9基因中HhaI多态性的变性梯度凝胶电泳（DGGE）检测
Nucleic Acids Res. 1990 Aug 25;18(16):4960. doi: 10.1093/nar/18.16.4960.
2
An HhaI polymorphism is present in factor IX genes of Asian subjects.
Hum Genet. 1990 Nov;86(1):87-8. doi: 10.1007/BF00205181.
3
Molecular analysis of factor IX gene in an Iranian female with severe hemophilia B.
Acta Haematol. 2008;119(3):151-3. doi: 10.1159/000128043. Epub 2008 Apr 24.
4
Detection of the Taq 1 polymorphism of the factor IX gene by P.C.R.通过聚合酶链反应检测凝血因子IX基因的Taq 1多态性
Thromb Res. 1991 Jun 1;62(5):599-601. doi: 10.1016/0049-3848(91)90033-s.
5
Carrier detection and prenatal diagnosis of hemophilia B with more advanced techniques.采用更先进技术进行B型血友病的携带者检测和产前诊断。
Ann Hematol. 1993 Dec;67(6):289-93. doi: 10.1007/BF01696349.
6
[Sal I, Nru I and Mse I restriction fragment length polymorphisms of factor IX gene in Chinese Han people].[中国人凝血因子IX基因Sal I、Nru I和Mse I限制性片段长度多态性]
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2002 Jun;10(3):247-50.
7
[A PCR-system of analyzing polymorphic markers in gamma-A and gamma-G globin genes and gene for human blood coagulation factor IX with an internal control of the completeness of restriction hydrolysis].
Genetika. 1993 Mar;29(3):388-92.
8
Human ApoCI HpaI restriction site polymorphism revealed by the polymerase chain reaction.通过聚合酶链反应揭示的人类载脂蛋白CⅠ HpaⅠ限制性酶切位点多态性
Nucleic Acids Res. 1990 Jun 11;18(11):3428. doi: 10.1093/nar/18.11.3428-a.
9
Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX.
Hum Genet. 1985;71(2):122-6. doi: 10.1007/BF00283366.
10
[Search for the carrier state of hemophilia B using restriction fragment length polymorphism].[利用限制性片段长度多态性检测B型血友病携带者状态]
Ned Tijdschr Geneeskd. 1985 Jun 15;129(24):1141-5.

引用本文的文献

1
Carrier detection and prenatal diagnosis of hemophilia B with more advanced techniques.采用更先进技术进行B型血友病的携带者检测和产前诊断。
Ann Hematol. 1993 Dec;67(6):289-93. doi: 10.1007/BF01696349.

本文引用的文献

1
Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.通过聚合酶链反应将一段40个碱基对的富含G + C的序列（GC夹）连接到基因组DNA片段上，可提高对单碱基变化的检测。
Proc Natl Acad Sci U S A. 1989 Jan;86(1):232-6. doi: 10.1073/pnas.86.1.232.

DGGE detection of HhaI polymorphism in the F9 gene.

作者信息

Caprino D, Acquila M, Pecorara M, Mori P G

机构信息

Department of Pediatric Hematology/Oncology, G. Gaslini Children's Hospital, Genoa, Italy.

出版信息

Nucleic Acids Res. 1990 Aug 25;18(16):4960. doi: 10.1093/nar/18.16.4960.

DOI:10.1093/nar/18.16.4960
PMID:1975673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC332026/
Abstract
摘要