• 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

A case of XX male syndrome.

作者信息

Lisker R, Flores F, Cobo A, Rojas F G

出版信息

J Med Genet. 1970 Dec;7(4):394-8. doi: 10.1136/jmg.7.4.394.

DOI:10.1136/jmg.7.4.394
PMID:5501706
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1468937/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/3e3429d7098e/jmedgene00371-0095-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/4a18bedea86a/jmedgene00371-0092-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/e450ced25d4d/jmedgene00371-0093-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/f7d9f94a31e6/jmedgene00371-0093-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/894e2745c5ac/jmedgene00371-0094-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/3e3429d7098e/jmedgene00371-0095-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/4a18bedea86a/jmedgene00371-0092-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/e450ced25d4d/jmedgene00371-0093-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/f7d9f94a31e6/jmedgene00371-0093-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/894e2745c5ac/jmedgene00371-0094-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aec/1468937/3e3429d7098e/jmedgene00371-0095-a.jpg

相似文献

1
A case of XX male syndrome.一例XX男性综合征病例。
J Med Genet. 1970 Dec;7(4):394-8. doi: 10.1136/jmg.7.4.394.
2
The sex reversal syndrome (the XX male patient).性反转综合征(XX男性患者)
J Urol. 1985 Jul;134(1):152-3. doi: 10.1016/s0022-5347(17)47036-4.
3
[A further case of a male individual with a 46,XX karyotype].[一名核型为46,XX的男性个体的另一病例]
Ann Genet. 1974 Sep;17(3):201-9.
4
A South African Indian hermaphrodite.
S Afr Med J. 1974 Jun 9;48(31):1349-50.
5
[Testicular feminization with ambosexualization at puberty and 46 XY-47 XXY mosaicism].
Ann Endocrinol (Paris). 1972 Nov-Dec;33(6):607-21.
6
[Two observations of men 46,XX].对46,XX男性的两项观察
Ann Genet. 1967 Dec;10(4):193-200.
7
A clinical and cytogenetical study of XX male.XX男性的临床与细胞遗传学研究
Hereditas. 1969;62(3):285-92. doi: 10.1111/j.1601-5223.1969.tb02238.x.
8
[Males with karyotype 46 XX. 2 new cases].
Ann Endocrinol (Paris). 1969 Nov-Dec;30(6):741-58.
9
Unusual dual genital duct remnants in true hermaphroditism.真两性畸形中不寻常的双生殖管道残留
J Med Genet. 1988 Mar;25(3):206-8. doi: 10.1136/jmg.25.3.206.
10
[Male hermaphroditism, its pathogenesis and classification].[男性两性畸形,其发病机制与分类]
Ginekol Pol. 1969 Jul;40(7):779-87.

本文引用的文献

1
STERILE MALE WITH THE CHROMOSOME CONSTITUTION 46 XX.染色体组成为46 XX的不育男性。
Cytogenetics. 1964;3:207-18. doi: 10.1159/000129812.
2
XX SEX CHROMOSOMES IN A HUMAN MALE. FIRST CASE.人类男性中的XX性染色体。首例。
Acta Med Scand. 1964;175:SUPPL 412:25-8. doi: 10.1111/j.0954-6820.1964.tb04630.x.
3
Klinefelter's syndrome, a clinical and cytogenetic study in twenty-four cases.
Acta Endocrinol (Copenh). 1967;54:Suppl 113:5+. doi: 10.1530/acta.0.054s005.
4
XXY cells in a predominantly XX human male: evidence for cell selection.
Pediatrics. 1966 Dec;38(6):982-5.
5
[Female chromosome set in a male without testicular tubules].[无睾丸小管男性的女性染色体组型]
Dtsch Med Wochenschr. 1966 Dec 2;91(48):2159-65. doi: 10.1055/s-0028-1111657.
6
[Klinefelter's syndrome with 46-XX karyotype at the cutaneous, blood and testicular levels].
Ann Endocrinol (Paris). 1965 Nov-Dec;26(6):727-38.
7
Significance of sex chromosome derived heterochromatin in mammals.
Nature. 1968 Aug 31;219(5157):910-4. doi: 10.1038/219910a0.
8
Dermatoglyphic patterns in a sample of normal urban Mexicans.墨西哥城市正常人群样本中的皮纹模式。
Hum Hered. 1969;19(5):534-9. doi: 10.1159/000152264.
9
[Two observations of men 46,XX].对46,XX男性的两项观察
Ann Genet. 1967 Dec;10(4):193-200.
10
X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome.真性两性畸形和XX克兰费尔特综合征病因中的X-Y染色体互换
Lancet. 1966 Aug 27;2(7461):475-6. doi: 10.1016/s0140-6736(66)92778-4.