• 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

关于中度智力迟钝的疾病分类学,特别关注X连锁智力迟钝。对274名住院中度智力迟钝男性进行的诊断性基因调查。

On the nosology of moderate mental retardation with special attention to X-linked mental retardation. A diagnostic genetic survey of 274 institutionalized moderately mentally retarded men.

作者信息

Volcke P, Dereymaeker A M, Fryns J P, van den Berghe H

机构信息

Center for Human Genetics, University of Leuven, Belgium.

出版信息

Genet Couns. 1990;1(1):47-56.

PMID:2222922
Abstract

In this paper we report the results of a genetic-diagnostic survey of 274 institutionalized moderately mentally retarded adult males and compare these data with those from our previous studies in the severely mentally retarded and from a comparable population of 262 institutionalized moderately mentally retarded males and females (The Borgenstein experience). Special attention is paid to the nosology of X-linked mental retardation and familial mental retardation in general.

摘要

在本文中,我们报告了对274名机构收容的中度智力迟钝成年男性进行基因诊断调查的结果,并将这些数据与我们之前对重度智力迟钝者以及来自262名机构收容的中度智力迟钝男性和女性的可比人群(博根斯坦研究)的研究数据进行比较。我们特别关注X连锁智力迟钝和一般家族性智力迟钝的疾病分类学。

相似文献

1
On the nosology of moderate mental retardation with special attention to X-linked mental retardation. A diagnostic genetic survey of 274 institutionalized moderately mentally retarded men.关于中度智力迟钝的疾病分类学,特别关注X连锁智力迟钝。对274名住院中度智力迟钝男性进行的诊断性基因调查。
Genet Couns. 1990;1(1):47-56.
2
A genetic diagnostic survey in an institutionalized population of 116 moderately to severely retarded male patients: the Rekem experience.对116名中重度智障男性患者的收容机构人群进行的基因诊断调查:雷肯经验。
Genet Couns. 1995;6(3):251-8.
3
Cytogenetic findings in moderate and severe mental retardation. A study of an institutionalized population of 1991 patients.
Acta Paediatr Scand Suppl. 1984;313:1-23.
4
A systematic cytogenetic study of a population of 1170 mentally retarded and/or behaviourly disturbed patients including fragile X-screening. The Hondsberg experience.对1170名智力迟钝和/或行为障碍患者进行的系统细胞遗传学研究,包括脆性X筛查。洪兹贝格经验。
J Genet Hum. 1988 Dec;36(5):425-46.
5
A genetic diagnostic survey in an institutionalized population of 262 moderately mentally retarded patients: the Borgerstein experience.对262名中度智力发育迟缓的住院患者进行的基因诊断调查:博尔格施泰因的经验。
J Ment Defic Res. 1990 Feb;34 ( Pt 1):29-40. doi: 10.1111/j.1365-2788.1990.tb01512.x.
6
The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers.一组有患病兄弟的中度智障男性中X连锁疾病的诊断与发病率
Am J Med Genet. 1983 Apr;14(4):713-24. doi: 10.1002/ajmg.1320140413.
7
A genetic-diagnostic survey in an institutionalized population of 158 mentally retarded patients. The Viaene experience.对158名智障患者收容机构人群进行的基因诊断调查。维亚内经历。
Clin Genet. 1988 Aug;34(2):126-34. doi: 10.1111/j.1399-0004.1988.tb02848.x.
8
Screening of mentally retarded males for macro-orchidism and the fragile X chromosome.
Am J Med Genet. 1983 Aug;15(4):631-5. doi: 10.1002/ajmg.1320150414.
9
[Chromosome X-linked mental retardation and marfanoid syndrome].[X染色体连锁智力迟钝与马方综合征样综合征]
J Genet Hum. 1988 Jan;36(1-2):123-8.
10
A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation.对307名智力迟钝、生活在收容机构的成年男性患者进行的临床、细胞遗传学和家族研究,特别关注脆性X染色体阴性的X连锁智力迟钝。
Clin Genet. 1991 Jun;39(6):434-41. doi: 10.1111/j.1399-0004.1991.tb03055.x.