• 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
Combined first trimester screen or noninvasive prenatal testing or both.孕早期联合筛查或无创产前检测或两者皆用。
Singapore Med J. 2015 Jan;56(1):1-3. doi: 10.11622/smedj.2015001.
2
First-trimester screening markers are altered in pregnancies conceived after IVF/ICSI.体外受精/卵胞浆内单精子注射后妊娠的孕早期筛查标志物会发生改变。
Ultrasound Obstet Gynecol. 2009 Jan;33(1):8-17. doi: 10.1002/uog.6254.
3
Development of medians generators for the calculation of MoM for the first-trimester Down syndrome maternal serum markers.
Ann Biol Clin (Paris). 2016 Jun 1;74(3):293-8. doi: 10.1684/abc.2016.1146.
4
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis.跨孕期检测在选择高危孕妇进行侵入性产前诊断中的有效性。
Prenat Diagn. 2010 Aug;30(8):795-6. doi: 10.1002/pd.2539.
5
Performance of first-trimester serum screening for trisomy 21 before and from 11 + 0 weeks of gestational age in The Netherlands.
Prenat Diagn. 2010 Sep;30(9):906-8. doi: 10.1002/pd.2581.
6
First-trimester Down syndrome screening using additional serum markers with and without nuchal translucency and cell-free DNA.使用额外血清标志物联合或不联合颈部透明带及游离DNA进行孕早期唐氏综合征筛查。
Prenat Diagn. 2013 Nov;33(11):1044-9. doi: 10.1002/pd.4194. Epub 2013 Aug 6.
7
More invasive procedures are done to detect each case of Down's syndrome in younger women.更具侵入性的检查手段被用于检测年轻女性中的每一例唐氏综合征。
Acta Obstet Gynecol Scand. 2011 Jun;90(6):642-7. doi: 10.1111/j.1600-0412.2011.01113.x. Epub 2011 Apr 15.
8
First-trimester Down syndrome screening: free beta-human chorionic gonadotropin and pregnancy-associated plasma protein A.孕早期唐氏综合征筛查:游离β-人绒毛膜促性腺激素和妊娠相关血浆蛋白A
Am J Obstet Gynecol. 1996 Feb;174(2):612-6. doi: 10.1016/s0002-9378(96)70436-2.
9
First-trimester or second-trimester screening, or both, for Down's syndrome.孕早期或孕中期唐氏综合征筛查,或两者皆做。
N Engl J Med. 2005 Nov 10;353(19):2001-11. doi: 10.1056/NEJMoa043693.
10
[Trisomy 21 screening: value of ultrasound and serum markers in a combined approach].[21三体综合征筛查:超声与血清标志物联合应用的价值]
J Gynecol Obstet Biol Reprod (Paris). 2001 Feb;30(1):11-27.

引用本文的文献

1
Scoping review: the current landscape of NIPT in South Africa.综述:南非无创产前检测的现状
J Community Genet. 2025 May 28. doi: 10.1007/s12687-025-00802-6.
2
Economic evaluation of prenatal screening for fetal aneuploidies in Thailand.泰国胎儿非整倍体产前筛查的经济评价。
PLoS One. 2023 Sep 15;18(9):e0291622. doi: 10.1371/journal.pone.0291622. eCollection 2023.
3
Whole-Chromosome Karyotyping of Fetal Nucleated Red Blood Cells Using the Ion Proton Sequencing Platform.利用 Ion Proton 测序平台对胎儿有核红细胞进行全染色体组染色体核型分析。
Genes (Basel). 2022 Nov 30;13(12):2257. doi: 10.3390/genes13122257.
4
Prenatal screening in the era of non-invasive prenatal testing: a Nationwide cross-sectional survey of obstetrician knowledge, attitudes and clinical practice.无创产前检测时代的产前筛查:一项关于产科医生知识、态度和临床实践的全国性横断面调查。
BMC Pregnancy Childbirth. 2020 Oct 1;20(1):579. doi: 10.1186/s12884-020-03279-y.
5
Noninvasive prenatal testing in routine clinical practice for a high-risk population: Experience from a center.高危人群常规临床实践中的无创产前检测:来自一个中心的经验
Medicine (Baltimore). 2016 Oct;95(41):e5126. doi: 10.1097/MD.0000000000005126.

本文引用的文献

1
The assessment of combined first trimester screening in women of advanced maternal age in an Asian cohort.亚洲队列中高龄孕产妇孕早期联合筛查的评估
Singapore Med J. 2015 Jan;56(1):47-52. doi: 10.11622/smedj.2015009.
2
Performance of screening for aneuploidies by cell-free DNA analysis of maternal blood in twin pregnancies.双胎妊娠中通过孕妇血液游离DNA分析进行非整倍体筛查的性能
Ultrasound Obstet Gynecol. 2015 Jan;45(1):61-6. doi: 10.1002/uog.14690. Epub 2014 Dec 4.
3
Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing.应用半导体测序技术进行常见非整倍体的无创性产前诊断。
Proc Natl Acad Sci U S A. 2014 May 20;111(20):7415-20. doi: 10.1073/pnas.1321997111. Epub 2014 May 5.
4
DNA sequencing versus standard prenatal aneuploidy screening.DNA 测序与标准产前非整倍体筛查。
N Engl J Med. 2014 Feb 27;370(9):799-808. doi: 10.1056/NEJMoa1311037.
5
Replacing the combined test by cell-free DNA testing in screening for trisomies 21, 18 and 13: impact on the diagnosis of other chromosomal abnormalities.在21、18和13三体综合征筛查中用游离DNA检测取代联合检测:对其他染色体异常诊断的影响。
Fetal Diagn Ther. 2014;35(3):174-84. doi: 10.1159/000358388. Epub 2014 Feb 8.
6
Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.应用母体外周血游离 DNA 低深度全基因组测序技术进行非侵入性产前检测胎儿染色体非整倍体:单中心 1982 例连续病例的回顾性研究
Ultrasound Obstet Gynecol. 2014 Mar;43(3):254-64. doi: 10.1002/uog.13277. Epub 2014 Feb 10.
7
Prevention of perinatal death and adverse perinatal outcome using low-dose aspirin: a meta-analysis.使用低剂量阿司匹林预防围产期死亡和不良围产期结局:一项荟萃分析。
Ultrasound Obstet Gynecol. 2013 May;41(5):491-9. doi: 10.1002/uog.12421.
8
Chronotherapy with low-dose aspirin for prevention of complications in pregnancy.低剂量阿司匹林的时辰治疗用于预防妊娠并发症。
Chronobiol Int. 2013 Mar;30(1-2):260-79. doi: 10.3109/07420528.2012.717455. Epub 2012 Sep 24.
9
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.基于母体外周血游离 DNA 测序的全基因组胎儿非整倍体检测
Obstet Gynecol. 2012 May;119(5):890-901. doi: 10.1097/AOG.0b013e31824fb482.
10
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.母体外周血游离 DNA 的选择性分析用于评估胎儿三体性。
Prenat Diagn. 2012 Jan;32(1):3-9. doi: 10.1002/pd.2922. Epub 2012 Jan 6.

Combined first trimester screen or noninvasive prenatal testing or both.

作者信息

Tan Tony Yew Teck

机构信息

Raffles Women's Centre, Raffles Hospital, 585 North Bridge Road, Singapore 188770.

出版信息

Singapore Med J. 2015 Jan;56(1):1-3. doi: 10.11622/smedj.2015001.

DOI:10.11622/smedj.2015001
PMID:25640091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4325569/
Abstract
摘要