• 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

儿童精神科患者的微小染色体变异

Minor chromosome variants in child psychiatric patients.

作者信息

Funderburk S J, Guthrie D, Lind R C, Muller H M, Sparkes R S, Westlake J R

出版信息

Am J Med Genet. 1978;1(3):301-8. doi: 10.1002/ajmg.1320010306.

DOI:10.1002/ajmg.1320010306
PMID:677169
Abstract

The frequency of minor chromosome variants, as detected by conventional chromosome analysis, was examined among 1,289 child psychiatric patients, of whom one-fourth had only behavioral problems and three-fourths had congenital abnormalities and more severe mental disorders. There was no more than random association between prominent satellites, prominent secondary constrictions or a long Y chromosome, and congenital abnormalities or more severe mental disorders. The frequencies of these chromosome variants were affected by race as has been shown in previous studies. These findings do not support the evidence for a developmental effect of minor variants in man.

摘要

通过传统染色体分析检测到的微小染色体变异频率,在1289名儿童精神病患者中进行了检查,其中四分之一仅有行为问题,四分之三有先天性异常和更严重的精神障碍。显著卫星、显著次缢痕或长Y染色体与先天性异常或更严重的精神障碍之间不存在超过随机的关联。这些染色体变异的频率如先前研究所示受种族影响。这些发现不支持人类微小变异具有发育效应的证据。

相似文献

1
Minor chromosome variants in child psychiatric patients.儿童精神科患者的微小染色体变异
Am J Med Genet. 1978;1(3):301-8. doi: 10.1002/ajmg.1320010306.
2
Prominent satellites in oligophrenic, malformed patients: incidence, frequency of satellite associations and karyotype-phenotype comparisons.智力发育迟缓、畸形患者中的显著随体:发生率、随体关联频率及核型-表型比较
Acta Anthropogenet. 1982;6(1):69-84.
3
Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay.使用传统细胞遗传学和多重荧光原位杂交端粒(M-TEL)完整性检测法对30例病因不明的发育迟缓、畸形特征或先天性异常患者进行研究。
Hum Genet. 2002 Jul;111(1):31-9. doi: 10.1007/s00439-002-0739-x. Epub 2002 Jun 13.
4
Cytogenetic findings in 200 children with mental retardation and multiple congenital anomalies of unknown cause.200例病因不明的智力发育迟缓及多发先天性异常患儿的细胞遗传学研究结果
Am J Med Genet. 1982 Jun;12(2):155-73. doi: 10.1002/ajmg.1320120206.
5
XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning.XYY综合征及其他Y染色体多体性。精神状态与社会心理功能。
Genet Couns. 1995;6(3):197-206.
6
Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.在患有特发性智力障碍和畸形特征的患者中检测到的亚端粒染色体重排。
Genet Couns. 2005;16(2):129-38.
7
Chromosomal abnormalities in a psychiatric population.精神疾病人群中的染色体异常。
Am J Med Genet. 1995 Feb 27;60(1):53-4. doi: 10.1002/ajmg.1320600110.
8
[Karyotypes with 2 Y chromosomes and behavior disorders].具有两条Y染色体的核型与行为障碍
Ann Med Psychol (Paris). 1967 Jan;125(1):116-26.
9
Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:).新发8p末端缺失(8pter----8p23.1)导致正常表型和轻度智力发育迟缓。
Ann Genet. 1989;32(3):171-3.
10
Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.13号染色体长臂32区“关键区域”的初步定义:14例13q缺失病例报告及文献综述
Am J Med Genet. 1993 Jan 1;45(1):52-9. doi: 10.1002/ajmg.1320450115.

引用本文的文献

1
Chromosome variants in children referred for cytogenetic examination from two paediatric departments during a 12-year-period.在12年期间,从两个儿科科室转来进行细胞遗传学检查的儿童中的染色体变异。
Hum Genet. 1980;56(1):67-9. doi: 10.1007/BF00281571.
2
Inverted Y chromosome polymorphism in the Gujerati Muslim Indian population of South Africa.
Hum Genet. 1986 Nov;74(3):223-9. doi: 10.1007/BF00282538.
3
Prominent acrocentric chromosome satellites in child patients with mental retardation or psychiatric disorders; no IQ-satellite size correlation.患有智力障碍或精神疾病的儿童患者中显著的近端着丝粒染色体随体;智商与随体大小无相关性。
Hum Genet. 1979;50(2):179-85. doi: 10.1007/BF00390239.