• 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

一名患有10号染色体长臂末端缺失的男孩的精神、心理及行为功能状况

The psychiatric, psychological and behavioural functioning of a boy with terminal deletion of the long arm of chromosome 10.

作者信息

Turk J, Christie D, Sales J, Surtees R

机构信息

Behavioural Sciences Unit, Institute of Child Health, London.

出版信息

Dev Med Child Neurol. 1993 May;35(5):439-48. doi: 10.1111/j.1469-8749.1993.tb11667.x.

DOI:10.1111/j.1469-8749.1993.tb11667.x
PMID:7684347
Abstract

The developmental and behavioural functioning of a six-year-old boy with deletion of the long arm of chromosome 10 was evaluated using reliable, standardised, psychological inventories. The information obtained clarified his complex pattern of strengths and needs; it also contributes scientifically derived data to the literature on behavioural correlates of this condition.

摘要

一名10号染色体长臂缺失的六岁男孩的发育和行为功能,通过可靠、标准化的心理量表进行了评估。所获得的信息明确了他复杂的优势和需求模式;它还为关于这种情况的行为相关性的文献提供了科学得出的数据。

相似文献

1
The psychiatric, psychological and behavioural functioning of a boy with terminal deletion of the long arm of chromosome 10.一名患有10号染色体长臂末端缺失的男孩的精神、心理及行为功能状况
Dev Med Child Neurol. 1993 May;35(5):439-48. doi: 10.1111/j.1469-8749.1993.tb11667.x.
2
The partial monosomy 10q syndrome: report on two patients and review of the developmental data.10q部分单体综合征:两例患者报告及发育数据综述
J Ment Defic Res. 1991 Jun;35 ( Pt 3):259-67. doi: 10.1111/j.1365-2788.1991.tb01059.x.
3
Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays.涉及9p部分三体和Yq部分单体的不平衡易位伴神经发育迟缓。
J Child Neurol. 2013 Apr;28(4):524-6. doi: 10.1177/0883073812446309. Epub 2012 Jun 29.
4
Congenital indifference to pain and deletion of chromosome 10q-: new association.
J Child Neurol. 2006 Feb;21(2):174-7. doi: 10.1177/08830738060210022001.
5
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.腭心面综合征(VCFS)的行为表型:从婴儿期到青春期
Genet Couns. 1999;10(1):79-88.
6
IgA deficiency associated with growth hormone deficiency in a boy with short arm deletion of chromosome 18 (46,XY,18p-).一名患有18号染色体短臂缺失(46,XY,18p-)的男孩,其IgA缺乏与生长激素缺乏相关。
Ann Genet. 1994;37(2):82-5.
7
Neurodevelopmental and behavioral abnormalities associated with deletion of chromosome 9p.与9号染色体短臂缺失相关的神经发育和行为异常。
J Child Neurol. 2002 Jan;17(1):50-1. doi: 10.1177/088307380201700113.
8
Delayed myelination in a patient with 18q- syndrome.一名患有18号染色体长臂缺失综合征患者的髓鞘形成延迟。
Pediatr Neurol. 1994 Jul;11(1):64-7. doi: 10.1016/0887-8994(94)90095-7.
9
Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26).因母亲染色体易位导致的10q部分单体和9q部分三体伴肛门闭锁:t(9;10)(q32;q26)
Clin Genet. 1996 Oct;50(4):220-2. doi: 10.1111/j.1399-0004.1996.tb02630.x.
10
Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation.
Clin Genet. 1997 Jan;51(1):71-4. doi: 10.1111/j.1399-0004.1997.tb02420.x.