• 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

Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.

作者信息

Pang S, Pollack M S, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New M I

出版信息

Ann N Y Acad Sci. 1985;458:111-29. doi: 10.1111/j.1749-6632.1985.tb14597.x.

DOI:10.1111/j.1749-6632.1985.tb14597.x
PMID:3879117
Abstract
摘要

相似文献

1
Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
Ann N Y Acad Sci. 1985;458:111-29. doi: 10.1111/j.1749-6632.1985.tb14597.x.
2
Pitfalls in prenatal diagnosis of 21-hydroxylase deficiency by amniotic fluid steroid analysis? A six years experience in 102 pregnancies at risk.通过羊水类固醇分析进行21-羟化酶缺乏症的产前诊断存在哪些陷阱？对102例有风险妊娠的六年经验总结。
Ann N Y Acad Sci. 1985;458:130-47. doi: 10.1111/j.1749-6632.1985.tb14598.x.
3
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by amniotic fluid steroid analysis.
Prenat Diagn. 1982 Apr;2(2):97-102. doi: 10.1002/pd.1970020204.
4
[Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis].[21-羟化酶缺乏所致肾上腺增生：产前诊断与治疗。新生儿诊断]
Rev Med Liege. 1986 Jan 15;41(2):37-44.
5
[Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency].[21-羟化酶缺乏所致肾上腺皮质增生症的遗传咨询与产前诊断]
Presse Med. 1984 Apr 21;13(17):1087-90.
6
Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.21-羟化酶缺乏所致先天性肾上腺皮质增生症的产前治疗。
N Engl J Med. 1990 Jan 11;322(2):111-5. doi: 10.1056/NEJM199001113220207.
7
Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probes.
Prenat Diagn. 1989 Jul;9(7):457-66. doi: 10.1002/pd.1970090702.
8
Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluid.通过羊水21-脱氧皮质醇和17-羟孕酮的同步放射免疫测定法对21-羟化酶缺乏症先天性肾上腺皮质增生症进行产前诊断。
J Clin Endocrinol Metab. 1988 Mar;66(3):534-7. doi: 10.1210/jcem-66-3-534.
9
The use of gamma interferon to increase HLA antigen expression on cultured amniotic cells used for the prenatal diagnosis of 21-hydroxylase deficiency.使用γ干扰素增加用于21-羟化酶缺乏症产前诊断的培养羊膜细胞上的HLA抗原表达。
Ann N Y Acad Sci. 1985;458:148-55. doi: 10.1111/j.1749-6632.1985.tb14599.x.
10
First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.通过与HLA - DNA探针的连锁分析及17 - 羟孕酮测定对孕早期21 - 羟化酶缺乏症进行产前诊断。
Hum Genet. 1986 Aug;73(4):358-64. doi: 10.1007/BF00279101.

引用本文的文献

1
Prenatal diagnosis of congenital adrenal hyperplasia: reliability of amniotic fluid steroid analysis.先天性肾上腺皮质增生症的产前诊断：羊水类固醇分析的可靠性
J Med Genet. 1987 Jun;24(6):344-7. doi: 10.1136/jmg.24.6.344.
2
Prenatal diagnosis and management of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.因类固醇21-羟化酶缺乏所致先天性肾上腺皮质增生症的产前诊断与管理
Indian J Pediatr. 1988 Jul-Aug;55(4):472-5. doi: 10.1007/BF02868427.
3
First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.
通过与HLA - DNA探针的连锁分析及17 - 羟孕酮测定对孕早期21 - 羟化酶缺乏症进行产前诊断。
Hum Genet. 1986 Aug;73(4):358-64. doi: 10.1007/BF00279101.