• 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

Prenatal diagnosis of trisomy 22 at the first trimester of pregnancy.

作者信息

Xu Bi-Qiu, Jiang Xiao-Cui, Wan Li, Wang Sha, Yang Yan-Dong, Li Dong-Zhi

机构信息

Huadu District Maternal and Neonatal Healthcare Hospital of Guangzhou, Hu Zhong Hospital, Guangzhou, Guangdong, China.

Department of Ultrasound, The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.

出版信息

J Obstet Gynaecol. 2020 Apr;40(3):440-442. doi: 10.1080/01443615.2019.1606788. Epub 2019 Jul 25.

DOI:10.1080/01443615.2019.1606788
PMID:31340704
Abstract
摘要

相似文献

1
Prenatal diagnosis of trisomy 22 at the first trimester of pregnancy.妊娠早期22三体综合征的产前诊断。
J Obstet Gynaecol. 2020 Apr;40(3):440-442. doi: 10.1080/01443615.2019.1606788. Epub 2019 Jul 25.
2
Prenatal diagnosis of trisomy 9.三体 9 的产前诊断。
Singapore Med J. 2011 Jul;52(7):e150-2.
3
A CASE OF CONFINED PLACENTAL MOSAICISM WITH TRISOMY 15 ASSOCIATED WITH TURNER SYNDROME.一例与特纳综合征相关的15号染色体三体局限型胎盘嵌合体病例。
Genet Couns. 2016;27(4):485-488.
4
Prenatal diagnosis of double trisomy 48,XXX,+18 in the first trimester.孕早期48,XXX,+18双三体的产前诊断
J Ultrasound Med. 2005 May;24(5):717-9. doi: 10.7863/jum.2005.24.5.717.
5
Trisomy 18: first-trimester nuchal translucency with pathological correlation.18三体综合征:孕早期颈部透明带厚度测量及其病理相关性
Ultrasound Obstet Gynecol. 1995 Jan;5(1):55-6. doi: 10.1046/j.1469-0705.1995.05010055.x.
6
Trends in timing of prenatal diagnosis and abortion for fetal chromosomal abnormalities.胎儿染色体异常产前诊断及流产时间的趋势
Am J Obstet Gynecol. 2015 Oct;213(4):545.e1-4. doi: 10.1016/j.ajog.2015.06.008. Epub 2015 Jun 10.
7
Distinctive pattern of first trimester maternal serum biochemical markers in trisomy 22 pregnancies.22三体妊娠孕早期母体血清生化标志物的独特模式。
Prenat Diagn. 2008 Dec;28(12):1174-6. doi: 10.1002/pd.2134.
8
Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.无创产前检测在与宫内生长受限及22号染色体三体局限型胎盘嵌合相关的晚期妊娠中的应用
Taiwan J Obstet Gynecol. 2017 Oct;56(5):691-693. doi: 10.1016/j.tjog.2017.09.001.
9
Discordant results between fetal cell-free DNA in maternal plasma and chorionic villus sampling in a first-trimester fetus with increased nuchal translucency and megacystis.孕早期胎儿颈部透明带增厚及巨膀胱的病例中,母体血浆中胎儿游离DNA与绒毛取样结果不一致。
Ultrasound Obstet Gynecol. 2014 Sep;44(3):369. doi: 10.1002/uog.13412.
10
First trimester prenatal detection of mosaic trisomy 8.孕早期产前检测8号染色体嵌合三体。
J Obstet Gynaecol. 2021 Apr;41(3):484-486. doi: 10.1080/01443615.2019.1707174. Epub 2020 Feb 20.

引用本文的文献

1
Evaluating the Effectiveness of Quantitative Fluorescent Polymerase Chain Reaction as a Substitute or Complement to Conventional Karyotyping for Prenatal Diagnosis.评估定量荧光聚合酶链反应作为传统核型分析的替代或补充用于产前诊断的有效性。
J Obstet Gynaecol India. 2025 Apr;75(Suppl 1):422-429. doi: 10.1007/s13224-024-02032-1. Epub 2024 Jul 26.
2
Fetal cystic hygroma in the first trimester led to diagnosis of partial trisomy 22.孕早期胎儿颈部水囊瘤导致22号染色体部分三体综合征的诊断。
SAGE Open Med Case Rep. 2021 Feb 1;9:2050313X21991000. doi: 10.1177/2050313X21991000. eCollection 2021.