• 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

Familial true hermaphrodism in pre- and postpuberal genetic females; hormonal and morphologic studies.

作者信息

CLAYTON G W, SMITH J D, ROSENBERG H S

出版信息

J Clin Endocrinol Metab. 1958 Dec;18(12):1349-58. doi: 10.1210/jcem-18-12-1349.

DOI:10.1210/jcem-18-12-1349
PMID:13611019
Abstract
摘要

相似文献

1
Familial true hermaphrodism in pre- and postpuberal genetic females; hormonal and morphologic studies.
J Clin Endocrinol Metab. 1958 Dec;18(12):1349-58. doi: 10.1210/jcem-18-12-1349.
2
Familial true hermaphrodism.家族性真性两性畸形。
J Clin Endocrinol Metab. 1963 Feb;23:203-6. doi: 10.1210/jcem-23-2-203.
3
A case of true hermaphrodism: possible relationship to Klinefelter's syndrome.
J Clin Endocrinol Metab. 1957 Aug;17(8):1002-5. doi: 10.1210/jcem-17-8-1002.
4
Sex chromatin pattern in seminiferous tubule dysgenesis and other testicular disorders: relationship to true hermaphrodism and to Klinefelter's syndrome, with a review of gonadal ontogenesis.
J Clin Endocrinol Metab. 1957 Jun;17(6):703-36. doi: 10.1210/jcem-17-6-703.
5
True hermaphrodism. Review of literature and report of a case.
Plast Reconstr Surg. 1963 May;31:453-60.
6
Developmental aspects of human hermaphrodism: the significance of sex chromatin patterns.
J Clin Endocrinol Metab. 1957 May;17(5):676-92. doi: 10.1210/jcem-17-5-676.
7
Apparent masculinization of the female fetus diagnosed as true hermaphrodism by chromosomal studies.经染色体研究诊断为真两性畸形的女性胎儿出现明显男性化。
J Pediatr. 1962 Apr;60:540-4. doi: 10.1016/s0022-3476(62)80115-2.
8
Hermaphrodism; a case report.
J Kans Med Soc. 1950 Feb;51(2):60.
9
Hermaphrodism: recommendations concerning case management.雌雄同体：病例管理建议
J Clin Endocrinol Metab. 1956 Apr;16(4):547-56. doi: 10.1210/jcem-16-4-547.
10
[Clinical and biological study of a case of male pseudo-hermaphrodism].
Brux Med. 1953 Aug 23;33(34):1721-40.

引用本文的文献

1
[The significance of sex chromatin in cell nucleus morphological sex diagnosis with special reference to heterochromatic nuclear internal caps in leukocytes].[性染色质在细胞核形态学性别诊断中的意义，特别提及白细胞中异染色质核内小体]
Klin Wochenschr. 1960 Mar 15;38:283-7. doi: 10.1007/BF01483936.
2
Absence of Y specific DNA sequences in two siblings with 46XX hermaphroditism.两名患有46XX两性畸形的同胞中Y特异性DNA序列缺失。
Arch Dis Child. 1989 Aug;64(8):1185-7. doi: 10.1136/adc.64.8.1185.
3
Familial true hermaphrodism in three siblings: clinical, cytogenetic, histological and hormonal studies.
Humangenetik. 1975 Sep 10;29(2):99-109. doi: 10.1007/BF00430346.