• 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

The syndrome of goldenhar affecting two siblings.

作者信息

Krause U

出版信息

Acta Ophthalmol (Copenh). 1970;48(3):494-9. doi: 10.1111/j.1755-3768.1970.tb03749.x.

DOI:10.1111/j.1755-3768.1970.tb03749.x
PMID:5536008
Abstract
摘要

相似文献

1
The syndrome of goldenhar affecting two siblings.患有戈尔登哈综合征的两兄弟姊妹。
Acta Ophthalmol (Copenh). 1970;48(3):494-9. doi: 10.1111/j.1755-3768.1970.tb03749.x.
2
Goldenhar's syndrome: two cases of oculo-auriculo-vertebral dysplasia occurring in full-blood Australian Aboriginal sisters.
Aust Paediatr J. 1970 Mar;6(1):213-4.
3
Goldenhar's syndrome: two cases of oculo-auriculo-vertebral dysplasia occurring in full-blood Australian aboriginal sisters.
Aust Paediatr J. 1970 Dec;6(4):213-4.
4
[Goldenhar's syndrome in twins].
Bull Soc Ophtalmol Fr. 1967 Dec;67(12):1135-45.
5
[Malformative aspects involving the 1st branchial arch. Report of 3 cases].
Minerva Med. 1972 Feb 7;63(9):490-6.
6
Coloboma of the iris and choroid and retinal detachment in oculo-auricular dysplasia (Goldenhar syndrome).
Eye Ear Nose Throat Mon. 1972 Oct;51(10):384-6.
7
Goldenhar syndrome.
Indian J Ophthalmol. 1973 Jun;21(2):84-7.
8
A case of Goldenhar syndrome associated with an inguinal hernia and extensive renal, ureteric, and bladder abnormalities.
St Lukes Hosp Gaz (Guardamangia). 1976 Jun;11(1):48-9.
9
[Syndrome of the 1st branchial arch].
Cesk Oftalmol. 1973 Mar;29(2):117-23.
10
[The syndromes of the first arch. Presentation of the syndrome of Goldenhar].
Bull Soc Ophtalmol Fr. 1976 Jan;76(1):95.

引用本文的文献

1
Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe.眼-耳-脊椎综合征的患病率、产前诊断及临床特征：一项基于欧洲登记处的研究
Eur J Hum Genet. 2014 Aug;22(8):1026-33. doi: 10.1038/ejhg.2013.287. Epub 2014 Jan 8.
2
A Lebanese family with autosomal recessive oculo-auriculo-vertebral (OAV) spectrum and review of the literature: is OAV a genetically heterogeneous disorder?一个患有常染色体隐性眼-耳-脊椎（OAV）谱系疾病的黎巴嫩家庭及文献综述：OAV是一种基因异质性疾病吗？
Appl Clin Genet. 2011 Jul 6;4:93-7. doi: 10.2147/TACG.S12643. Print 2011.
3
Hemifacial microsomia: from gestation to childhood.
半侧颜面短小畸形：从孕期到儿童期
J Craniofac Surg. 2009 Mar;20 Suppl 1(Suppl 1):664-9. doi: 10.1097/SCS.0b013e318193d5d5.
4
Goldenhar syndrome and hemifacial microsomia: observations on three patients.戈尔登哈综合征与半侧颜面短小畸形：三例患者观察报告
Eur J Pediatr. 1980 May;133(3):287-92. doi: 10.1007/BF00496092.
5
Familial occurrence of a syndrome with branchial dysplasia, mental deficiency, club feet, and inguinal herniae.一种伴有鳃发育异常、智力缺陷、畸形足和腹股沟疝的综合征的家族性发病情况。
J Med Genet. 1982 Jun;19(3):214-5. doi: 10.1136/jmg.19.3.214.
6
Autosomal dominant asymmetrical radial dysplasia, dysmorphic facies, and conductive hearing loss (facioauriculoradial dysplasia).常染色体显性不对称性桡骨发育不全、面部畸形和传导性听力损失（面耳桡骨发育不全）
J Med Genet. 1982 Apr;19(2):110-5. doi: 10.1136/jmg.19.2.110.
7
Genetic aspects of hemifacial microsomia.半侧颜面短小畸形的遗传学方面
Hum Genet. 1983;64(3):291-6. doi: 10.1007/BF00279415.
8
Empirical recurrence risk after unidentified multiple congenital abnormalities.未明确的多发先天性异常后的经验性复发风险
J Med Genet. 1983 Oct;20(5):367-71. doi: 10.1136/jmg.20.5.367.
9
Goldenhar's syndrome. Oculoauriculo-vertebral dysplasia.戈尔登哈综合征。眼耳脊椎发育不良。
Arch Dis Child. 1973 Jul;48(7):537-41. doi: 10.1136/adc.48.7.537.