• 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

连续自然流产,其中一次流产胎儿存在2号染色体间的全臂易位。

Successive spontaneous abortions including one with whole-arm translocation between chromosomes 2.

作者信息

Ohama K, Kusumi I, Takahara H, Kajii T

出版信息

Hum Genet. 1978 Jan 19;40(2):221-5. doi: 10.1007/BF00272305.

DOI:10.1007/BF00272305
PMID:624550
Abstract

A family with five induced and seven spontaneous abortions and no live births is described. Four of the seven spontaneous abortuses were available for cytogenetic examination and three were successfully karyotyped. Their karyotypes were 46,XX; 46,XX/46,XX,t(2;2)(2p2p;2q2q); and 46,XY. The karyotypes of the parents were normal. The origin of the 2p/2p and 2q/2q translocation in one of the abortuses was assigned to an interhomologous whole-arm translocation in an early mitotic division in a conceptus with a 46,XX karyotype.

摘要

本文描述了一个有5次人工流产和7次自然流产且无存活婴儿出生的家庭。7次自然流产中有4次可用于细胞遗传学检查,其中3次成功进行了核型分析。它们的核型分别为46,XX;46,XX/46,XX,t(2;2)(2p2p;2q2q);以及46,XY。父母的核型正常。其中一次流产胎儿中2p/2p和2q/2q易位的起源被认为是在一个核型为46,XX的孕体早期有丝分裂中发生的同源全臂易位。

相似文献

1
Successive spontaneous abortions including one with whole-arm translocation between chromosomes 2.连续自然流产,其中一次流产胎儿存在2号染色体间的全臂易位。
Hum Genet. 1978 Jan 19;40(2):221-5. doi: 10.1007/BF00272305.
2
Whole-arm translocation between homologous chromosomes 7 in a woman with successive spontaneous abortions.一名有多次自然流产史的女性,其7号同源染色体之间发生了全臂易位。
Hum Genet. 1983;63(1):85-6. doi: 10.1007/BF00285407.
3
Familial 5/14 translocation with triple X and 47,XY + 14q.伴有XXX和47,XY + 14q的家族性5/14易位
Clin Genet. 1981 Jul;20(1):40-3. doi: 10.1111/j.1399-0004.1981.tb01804.x.
4
Segregation and fertility analysis in an autosomal reciprocal translocation, t(1;8)(q41;q23.1).常染色体相互易位t(1;8)(q41;q23.1)的分离与育性分析
Am J Hum Genet. 1985 May;37(3):533-42.
5
Familial occurrence of chromosome 7/12 translocation.7号/12号染色体易位的家族性发生情况。
Clin Genet. 1980 Dec;18(6):445-9. doi: 10.1111/j.1399-0004.1980.tb01791.x.
6
Cytogenetic findings in 122 couples with recurrent abortions.122对复发性流产夫妇的细胞遗传学研究结果
Hum Genet. 1981;57(1):101-3. doi: 10.1007/BF00271179.
7
Pregnancy outcome when both members of a couple have balanced translocations.夫妻双方均有平衡易位时的妊娠结局
Obstet Gynecol. 1995 May;85(5 Pt 2):844-6. doi: 10.1016/0029-7844(94)00246-a.
8
A 22/22 translocation carrier with recurrent abortions demonstrated by a Giemsa banding technique,一名经吉姆萨显带技术证实的22/22易位携带者,有反复流产史
Hum Genet. 1976 Feb 29;31(2):243-5. doi: 10.1007/BF00296154.
9
Reproductive risk in mating between two translocation carriers: case report and review of the literature.两名易位携带者之间交配的生殖风险:病例报告及文献综述
Am J Med Genet. 1993 Jun 15;46(5):524-8. doi: 10.1002/ajmg.1320460513.
10
Reciprocal translocation with special reference to reproductive failure.特别是关于生殖失败的相互易位。
Hum Genet. 1980;55(3):303-7. doi: 10.1007/BF00290208.

引用本文的文献

1
Normal sperm in a 2;2 homologous male translocation carrier.正常精子 2;2 同源易位携带者。
J Assist Reprod Genet. 2012 Jul;29(7):665-8. doi: 10.1007/s10815-012-9770-6. Epub 2012 Apr 27.
2
Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q).
Am J Hum Genet. 1996 Nov;59(5):1114-8.
3
Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.一名生长发育迟缓儿童出现父源7号染色体短臂单亲等臂染色体和母源7号染色体长臂单亲等臂染色体。

本文引用的文献

1
Banding analysis of abnormal karyotypes in spontaneous abortion.自然流产中异常核型的染色体显带分析。
Am J Hum Genet. 1973 Sep;25(5):539-47.
2
Trypsin banding of Giemsa-stained chromosomes.吉姆萨染色染色体的胰蛋白酶显带
Lancet. 1972 Dec 16;2(7790):1311-2. doi: 10.1016/s0140-6736(72)92684-0.
3
Pseudomosaicism in cultured amniotic-fluid cells.培养的羊水细胞中的假镶嵌现象。
Am J Hum Genet. 1994 Aug;55(2):253-65.
4
Whole-arm translocation between homologous chromosomes 7 in a woman with successive spontaneous abortions.一名有多次自然流产史的女性,其7号同源染色体之间发生了全臂易位。
Hum Genet. 1983;63(1):85-6. doi: 10.1007/BF00285407.
5
Morphology alone does not make an isochromosome.仅形态学特征不足以判定等臂染色体。
Hum Genet. 1986 Mar;72(3):253-5. doi: 10.1007/BF00291889.
Lancet. 1971 Nov;2(7732):1037. doi: 10.1016/s0140-6736(71)90354-0.
4
Observations of de novo clones of cytogentically aberrant cells in primary fibroblast cell strains from phenotypically normal women.对表型正常女性原代成纤维细胞株中细胞遗传学异常细胞的新生克隆的观察。
Am J Hum Genet. 1975 Mar;27(2):190-7.
5
Cytogenetically marked clones in human fibroblasts cultured from normal subjects.从正常受试者培养的人成纤维细胞中的细胞遗传学标记克隆。
Somatic Cell Genet. 1976 Jan;2(1):55-62. doi: 10.1007/BF01539242.