• 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

Tetrasomy 9p: prenatal diagnosis and fetopathological findings in a second trimester male fetus.

作者信息

Van Hove J, Kleczkowska A, De Bruyn M, Bekaert J, Fryns J P

机构信息

Department of Pathology, Sint Imelda Hospital, Belgium.

出版信息

Ann Genet. 1994;37(3):139-42.

PMID:7847795
Abstract

In this report the authors describe the fetopathological findings in a second trimester male fetus with pure 9p tetrasomy. The prenatal diagnosis was based on the echographic finding of severe internal anomalies of the central nervous, cardiovascular and urogenital systems.

摘要

相似文献

1
Tetrasomy 9p: prenatal diagnosis and fetopathological findings in a second trimester male fetus.
Ann Genet. 1994;37(3):139-42.
2
Three cases of tetrasomy 9p.9号染色体短臂四体综合征三例。
Am J Med Genet. 2002 Dec 15;113(4):375-80. doi: 10.1002/ajmg.b.10826.
3
Prenatal diagnosis of occipital encephalocele, mega-cisterna magna, mesomelic shortening, and clubfeet associated with pure tetrasomy 20p.
Prenat Diagn. 2003 Feb;23(2):124-7. doi: 10.1002/pd.543.
4
Detection of tetrasomy 9p by chromosome microarray analysis and determination of maternal origin of the aberrant chromosome by quantitative fluorescent polymerase chain reaction in a second-trimester fetus with multiple anomalies on fetal ultrasound.通过染色体微阵列分析检测9号染色体短臂四体,并利用定量荧光聚合酶链反应确定中期妊娠胎儿超声检查发现多种异常时异常染色体的母源起源。
Taiwan J Obstet Gynecol. 2024 Sep;63(5):785-787. doi: 10.1016/j.tjog.2024.07.007.
5
Prenatal diagnosis and fetopathological findings in five fetuses with trisomy 9.5例9三体胎儿的产前诊断及胎儿病理检查结果
Am J Med Genet. 1995 Apr 10;56(3):247-51. doi: 10.1002/ajmg.1320560302.
6
Prenatal diagnosis and findings of tetrasomy 9p.9号染色体短臂四体的产前诊断及发现
J Obstet Gynaecol Res. 2015 Jul;41(7):997-1002. doi: 10.1111/jog.12706. Epub 2015 May 6.
7
Prenatal ultrasound findings in complete trisomy 9.9号染色体完全三体的产前超声检查结果
Ultrasound Obstet Gynecol. 2003 Nov;22(5):479-83. doi: 10.1002/uog.233.
8
Prenatal diagnosis by rapid aneuploidy detection and karyotyping: a prospective study of the role of ultrasound in 1589 second-trimester amniocenteses.通过快速非整倍体检测和核型分析进行产前诊断:一项关于超声在1589例孕中期羊膜穿刺术中作用的前瞻性研究。
Prenat Diagn. 2004 Oct;24(10):790-5. doi: 10.1002/pd.985.
9
Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.一名患有多种先天性异常的活产婴儿中的非嵌合性9号染色体短臂四体:病例报告及与9号染色体短臂三体的比较
Am J Med Genet. 1996 Jun 14;63(3):434-7. doi: 10.1002/(SICI)1096-8628(19960614)63:3<434::AID-AJMG4>3.0.CO;2-R.
10
Prenatal diagnosis of complete trisomy 9: a case report and review of the literature.9号染色体完全三体的产前诊断:一例病例报告及文献复习
Am J Perinatol. 2006 Feb;23(2):131-5. doi: 10.1055/s-2006-931804.

引用本文的文献

1
A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report.9p 三体嵌合体程度高,但除了染色体平衡精子的中度少精症外无其他临床表现:一例报告。
J Assist Reprod Genet. 2020 Mar;37(3):573-577. doi: 10.1007/s10815-020-01690-0. Epub 2020 Jan 24.
2
A Systematic Clinical Review of Prenatally Diagnosed Tetrasomy 9p.产前诊断9号染色体短臂四体的系统临床综述
Balkan J Med Genet. 2019 Aug 28;22(1):11-20. doi: 10.2478/bjmg-2019-0012. eCollection 2019 Jun.