• 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

相似文献

1
Dermatoglyphs and chromosome mosaicism in parents of children with trisomy 18.18三体综合征患儿父母的皮纹与染色体嵌合体
J Med Genet. 1980 Apr;17(2):142-3. doi: 10.1136/jmg.17.2.142.
2
Dermatoglyphic peculiarities in Down's syndrome detection of mosaicism and balanced translocation carriers.唐氏综合征中嵌合体和平衡易位携带者检测的皮纹特征
Hum Genet Suppl. 1981;2:41-56. doi: 10.1007/978-3-642-68006-9_4.
3
Discriminant functions and 21-trisomy mosaicism.
Ann Hum Genet. 1975 Oct;39(2):127-40. doi: 10.1111/j.1469-1809.1975.tb00115.x.
4
Dermatoglyphic studies in the parents of trisomy 21 children I. Distribution of dermatoglyphic discriminants.21三体综合征患儿父母的皮纹学研究I.皮纹鉴别指标的分布情况
Hum Hered. 1981;31(4):201-7. doi: 10.1159/000153208.
5
Dermatoglyphics in parents of children with trisomy 21. Evaluation of their interest in genetic counselling.21三体综合征患儿父母的皮纹学。对他们接受遗传咨询意愿的评估。
Clin Genet. 1979 Jan;15(1):78-84. doi: 10.1111/j.1399-0004.1979.tb02030.x.
6
[Clinical dermatoglyphic findings in Down's syndrome with chromosome mosaicism. (Mosaicism-mongolism)].[唐氏综合征染色体嵌合体的临床皮纹学发现。（嵌合体 - 先天愚型）]
Monatsschr Kinderheilkd (1902). 1967 Oct;115(10):516-22.
7
Dermatoglyphic studies in parents of children with trisomy 21: detection of hidden mosaicism and its role in genetic counselling.21三体综合征患儿父母的皮纹学研究：隐匿性嵌合体的检测及其在遗传咨询中的作用。
Prog Clin Biol Res. 1982;84:371-84.
8
Clinical experience with trisomies 18 and 13.18三体和13三体的临床经验。
J Med Genet. 1978 Feb;15(1):48-60. doi: 10.1136/jmg.15.1.48.
9
[Dermatoglyphic studies in parents of children with Down's syndrome. I. Digital patterns].
An Esp Pediatr. 1986 Aug;25(2):87-90.
10
A family with three sibs carrying trisomy 21.一个有三个携带21三体综合征患儿的家庭。
Ann Genet. 1975 Jun;18(2):111-6.

本文引用的文献

1
FINGER-PRINT PATTERNS IN MONGOLISM.蒙古症中的指纹模式
Ann Hum Genet. 1964 Mar;27:279-82. doi: 10.1111/j.1469-1809.1963.tb00796.x.
2
Topological classification of palmar dermatoglyphics.
J Ment Defic Res. 1970 Jun;14(2):111-28. doi: 10.1111/j.1365-2788.1970.tb01106.x.
3
Dermatoglyphic variation in the South Midlands.英格兰中南部地区的皮纹变化
Heredity (Edinb). 1972 Dec;29(3):293-305. doi: 10.1038/hdy.1972.94.
4
Dermatoglyphic characteristics of 21-trisomy mosaicism in relation to the fully developed syndrome and normality.21-三体嵌合型的皮纹特征与完全发育的综合征及正常情况的关系。
J Ment Defic Res. 1974 Sep;18(3):209-69. doi: 10.1111/j.1365-2788.1974.tb01237.x.
5
Investigation of 142 mosaic mongols and mosaic parents of mongols; cytogenetic analysis and maternal age at birth.对142例嵌合型蒙古症患者及蒙古症患者的嵌合型父母进行调查；细胞遗传学分析及母亲生育年龄。
J Ment Defic Res. 1974 Sep;18(3):199-208. doi: 10.1111/j.1365-2788.1974.tb01236.x.
6
Finger pattern combinations in normal individuals and in Down's syndrome.正常个体与唐氏综合征患者的指纹模式组合
Hum Biol. 1973 Dec;45(4):563-70.
7
Parental dermatoglyphics in Down's syndrome. A ten-year study.唐氏综合征患者的父母指纹：一项十年研究
J Med Genet. 1973 Dec;10(4):328-32. doi: 10.1136/jmg.10.4.328.
8
Dermatoglyphics in parents of children with trisomy 21. Evaluation of their interest in genetic counselling.21三体综合征患儿父母的皮纹学。对他们接受遗传咨询意愿的评估。
Clin Genet. 1979 Jan;15(1):78-84. doi: 10.1111/j.1399-0004.1979.tb02030.x.

18三体综合征患儿父母的皮纹与染色体嵌合体

Dermatoglyphs and chromosome mosaicism in parents of children with trisomy 18.

作者信息

Holmes-Siedle M, Kerr S, Lindenbaum R H, Bobrow M

出版信息

J Med Genet. 1980 Apr;17(2):142-3. doi: 10.1136/jmg.17.2.142.

DOI:10.1136/jmg.17.2.142
PMID:7381871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1048522/
Abstract

Parents of patients with Down's syndrome show dermatoglyphic features intermediate between the affected and the normal population. Dermatoglyphs were studied on the parents of 19 cases of trisomy 18, but no similar "intermediate" traits were discovered. The number of cases studied needs to be enlarged before it can definitely be stated that trisomies 18 and 21 differ in this respect.

摘要

唐氏综合征患者的父母表现出的皮纹特征介于患病群体和正常群体之间。对19例18三体综合征患者的父母进行了皮纹研究，但未发现类似的“中间”特征。在能够明确断定18三体和21三体在这方面存在差异之前，需要扩大研究病例的数量。