• 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

Polymerase chain reaction amplification from dried blood spots on Guthrie cards.

作者信息

Schwartz E I, Khalchitsky S E, Eisensmith R C, Woo S L

出版信息

Lancet. 1990 Sep 8;336(8715):639-40. doi: 10.1016/0140-6736(90)93446-v.

DOI:10.1016/0140-6736(90)93446-v
PMID:1975418
Abstract
摘要

相似文献

1
Polymerase chain reaction amplification from dried blood spots on Guthrie cards.从滤纸片上的干血斑进行聚合酶链反应扩增。
Lancet. 1990 Sep 8;336(8715):639-40. doi: 10.1016/0140-6736(90)93446-v.
2
High quality genome-wide genotyping from archived dried blood spots without DNA amplification.从无 DNA 扩增的存档干血斑中进行高质量的全基因组基因分型。
PLoS One. 2013 May 30;8(5):e64710. doi: 10.1371/journal.pone.0064710. Print 2013.
3
Accuracy of multiplexed Illumina platform-based single-nucleotide polymorphism genotyping compared between genomic and whole genome amplified DNA collected from multiple sources.比较从多个来源收集的基因组DNA和全基因组扩增DNA之间，基于Illumina多重平台的单核苷酸多态性基因分型的准确性。
Cancer Epidemiol Biomarkers Prev. 2006 Dec;15(12):2533-6. doi: 10.1158/1055-9965.EPI-06-0219.
4
Protein identification from dried nipple aspirate fluid on Guthrie cards using mass spectrometry.使用质谱法从干血滤纸片上的乳头抽吸液中鉴定蛋白质。
Mol Med Rep. 2015 Jul;12(1):159-64. doi: 10.3892/mmr.2015.3432. Epub 2015 Mar 5.
5
DNA analysis of cystic fibrosis in Brazil by direct PCR amplification from Guthrie cards.
Am J Med Genet. 1993 Jul 1;46(6):665-9. doi: 10.1002/ajmg.1320460612.
6
Whole Genome Amplification from Blood Spot Samples.血斑样本的全基因组扩增
Methods Mol Biol. 2015;1347:163-78. doi: 10.1007/978-1-4939-2990-0_12.
7
Single tube multiplex PCR detection of 27 cystic fibrosis mutations and 4 polymorphisms using neonatal blood samples collected on Guthrie cards.使用在格思里卡片上采集的新生儿血样对27种囊性纤维化突变和4种多态性进行单管多重PCR检测。
Ann Clin Lab Sci. 2003 Summer;33(3):243-50.
8
Finger prick blood testing in Leber hereditary optic neuropathy.莱伯遗传性视神经病变的手指采血检测
Br J Ophthalmol. 1993 May;77(5):311-2. doi: 10.1136/bjo.77.5.311.
9
Rapid PCR-based detection of Brugia malayi DNA from blood spots by DNA Detection Test Strips.
Trans R Soc Trop Med Hyg. 2001 Mar-Apr;95(2):169-70. doi: 10.1016/s0035-9203(01)90148-8.
10
Human polyomavirus DNA is not detected in Guthrie cards (dried blood spots) from children who developed acute lymphoblastic leukemia.在患急性淋巴细胞白血病儿童的Guthrie卡片（干血斑）中未检测到人类多瘤病毒DNA。
Med Pediatr Oncol. 2003 Apr;40(4):219-23. doi: 10.1002/mpo.10246.

引用本文的文献

1
Advances in Directly Amplifying Nucleic Acids from Complex Samples.直接从复杂样本中扩增核酸的进展。
Biosensors (Basel). 2019 Sep 30;9(4):117. doi: 10.3390/bios9040117.
2
Screening for novel PAX3 polymorphisms and risks of spina bifida.新型PAX3基因多态性筛查与脊柱裂风险
Birth Defects Res A Clin Mol Teratol. 2007 Jan;79(1):45-9. doi: 10.1002/bdra.20322.
3
Genes encoding catalytic subunits of protein kinase A and risk of spina bifida.编码蛋白激酶A催化亚基的基因与脊柱裂风险
Birth Defects Res A Clin Mol Teratol. 2005 Sep;73(9):591-6. doi: 10.1002/bdra.20175.
4
Amplification of Guthrie card DNA: effect of guanidine thiocyanate on binding of natural whole blood PCR inhibitors.格思里卡片DNA的扩增：硫氰酸胍对天然全血PCR抑制剂结合的影响
J Clin Lab Anal. 1997;11(2):87-93. doi: 10.1002/(sici)1098-2825(1997)11:2<87::aid-jcla4>3.0.co;2-h.
5
Diagnosis of DiGeorge syndrome in nuclei released from archival autoptic heart specimens using fluorescence in situ hybridization.利用荧光原位杂交技术对存档尸检心脏标本中释放的细胞核进行DiGeorge综合征的诊断。
Hum Genet. 1996 Apr;97(4):414-7. doi: 10.1007/BF02267058.
6
Analysis of five CFTR mutations in Hungarian cystic fibrosis patients.
J Inherit Metab Dis. 1996;19(3):378. doi: 10.1007/BF01799276.
7
Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variants.口腔颌面部裂隙、父母吸烟与转化生长因子-α基因变异
Am J Hum Genet. 1996 Mar;58(3):551-61.
8
Rapid and efficient PCR/StyI test for identification of common mutation R408W in phenylketonuria patients.用于鉴定苯丙酮尿症患者常见突变R408W的快速高效PCR/StyI检测
J Med Genet. 1993 Feb;30(2):153-4. doi: 10.1136/jmg.30.2.153.
9
Molecular diagnosis of some common genetic diseases in Russia and the former USSR: present and future.俄罗斯及前苏联一些常见遗传病的分子诊断：现状与未来
J Med Genet. 1993 Feb;30(2):141-6. doi: 10.1136/jmg.30.2.141.
10
Finger prick blood testing in Leber hereditary optic neuropathy.莱伯遗传性视神经病变的手指采血检测
Br J Ophthalmol. 1993 May;77(5):311-2. doi: 10.1136/bjo.77.5.311.