• 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

[STRUCTURAL AND NUMERICAL CHROMOSOME PATTERN (GROUP A AND E) IN A GIRL WITH THE PENDRED SYNDROME].

作者信息

HENI F, SIEBNER H

出版信息

Klin Wochenschr. 1963 Nov 1;41:1038-43. doi: 10.1007/BF01478090.

DOI:10.1007/BF01478090
PMID:14098335
Abstract
摘要

相似文献

1
[STRUCTURAL AND NUMERICAL CHROMOSOME PATTERN (GROUP A AND E) IN A GIRL WITH THE PENDRED SYNDROME].[一名患有彭德莱德综合征女孩的染色体结构和数量模式(A组和E组)]
Klin Wochenschr. 1963 Nov 1;41:1038-43. doi: 10.1007/BF01478090.
2
PARTIAL DELETION OF THE SHORT ARMS OF A CHROMOSOME OF THE 4-5 GROUP (DENVER).第4-5组(丹佛)染色体短臂的部分缺失
Arch Dis Child. 1965 Feb;40(209):82-5. doi: 10.1136/adc.40.209.82.
3
[PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. INDIVIDUALIZATION OF A NEW MORBID STATE].
Sem Hop. 1964 Apr 14;40:1069-79.
4
A BOY WITH XXXXY SEX CHROMOSOMES.一名患有XXXXY性染色体的男孩。
J Med Genet. 1964 Dec;1(2):95-101. doi: 10.1136/jmg.1.2.95.
5
[CHROMOSOMAL MOSAICISM: NORMAL-D-D, WITH MENTAL AND CORPOREAL DEVELOPMENTAL RETARDATION].[染色体镶嵌现象:正常-D-D型,伴有智力和身体发育迟缓]
C R Hebd Seances Acad Sci. 1964 Jun 1;258:5549-53.
6
[FAMILIAL SEGREGATION OF A 5-13 TRANSLOCATION DETERMINING PARTIAL MONOSOMY AND A TRISOMY OF THE SHORT ARM OF THE 5 CHROMOSOME: "CAT CRY" DISEASE AND ITS "RECEPROCAL"].[决定5号染色体短臂部分单体性和三体性的5-13易位的家族性分离:“猫叫”综合征及其“对应情况”]
C R Hebd Seances Acad Sci. 1964 Jun 8;258:5767-70.
7
Ring 1 chromosome and dwarfism--a possible syndrome.1 号环状染色体与侏儒症——一种可能的综合征。
J Pediatr. 1967 Nov;71(5):719-22. doi: 10.1016/s0022-3476(67)80211-7.
8
An asymmetric chromosome pair in group 4-5. Association with mental and physical retardation.4-5组中的一对不对称染色体。与智力和身体发育迟缓相关。
Am J Dis Child. 1966 Jan;111(1):90-5. doi: 10.1001/archpedi.1966.02090040126018.
9
Leukocyte anomaly, mental retardation, and dwarfism in a family with abnormal chromosomes.
J Pediatr. 1963 Jul;63:21-8. doi: 10.1016/s0022-3476(63)80298-x.
10
[THE XXXXY SYNDROME].[XXXXY综合征]
Arch Kinderheilkd. 1964 Feb;170:20-33.

本文引用的文献

1
Comparison of chromosome constitution in chronic myelocytic leukemia and other myeloproliferative disorders.
Blood. 1962 Oct;20:393-423.
2
[Chromosomal research on blood cells of a patient with Waldenstrom's macroglobulinemia].
Klin Wochenschr. 1962 Apr 1;40:342-4. doi: 10.1007/BF01732444.
3
[Study of karyotypes in Stein-Leventhal syndrome].[ Stein-Leventhal综合征的核型研究]
Ann Endocrinol (Paris). 1961 Nov-Dec;22:841-9.
4
[On a specific chromosomal anomaly in leukemia (the "minute" or Ph-1 chromosome")].
Munch Med Wochenschr. 1962 Aug 17;104:1493-6.
5
Chromosomal mosaic in a girl with some features of mongolism.
Cytogenetics. 1962;1:20-31. doi: 10.1159/000129710.
6
[Male Turnerian pseudohermaphroditism].
Sem Hop. 1962 May 20;38:1699-705.
7
[The hereditary syndrome of inner ear deafness and faulty iodine utilization with goiter].[内耳性耳聋伴甲状腺肿及碘利用障碍的遗传性综合征]
Dtsch Med Wochenschr. 1961 Dec 15;86:2421-8. doi: 10.1055/s-0028-1113108.
8
XY/XO mosaicism.
Lancet. 1962 Oct 13;2(7259):783-4.
9
Abnormal sex-hromosome complements and the Xg blood-group.异常性染色体组成与Xg血型
Lancet. 1963 Mar 23;1(7282):665. doi: 10.1016/s0140-6736(63)91298-4.
10
Male pseudohermaphroditism and chromosomal mosaicism.
Am J Dis Child. 1962 Aug;104:172-9. doi: 10.1001/archpedi.1962.02080030174011.