Stickler syndrome: report of four cases.
作者信息
Kulkarni M L, Sureshkumar C, George V G
机构信息
Department of Paediatrics, J.J.M. Medical College, Karnataka, India.
出版信息
Ann Dent. 1993 Winter;52(2):23-7.
PMID:8267375
Abstract
摘要
相似文献
1
Stickler syndrome: report of four cases.斯蒂克勒综合征：4例报告。
Ann Dent. 1993 Winter;52(2):23-7.
2
Prenatal diagnosis of Pierre-Robin sequence as part of Stickler syndrome.作为斯蒂克勒综合征一部分的皮埃尔-罗宾序列征的产前诊断。
Prenat Diagn. 2002 Jul;22(7):567-8. doi: 10.1002/pd.369.
3
[On the causal and morphological etiology of the Pierre Robin syndrome].[关于皮埃尔·罗宾综合征的病因及形态学病因学]
Dtsch Zahnarztl Z. 1966 Nov 1;21(11):1321-38.
4
[Stickler syndrome].[斯蒂克勒综合征]
Bol Med Hosp Infant Mex. 1986 Apr;43(4):250-5.
5
The Stickler syndrome (hereditary arthro-ophthalmopathy).斯-韦二氏综合征（遗传性关节眼病）。
Clin Genet. 1977 Sep;12(3):179-82. doi: 10.1111/j.1399-0004.1977.tb00921.x.
6
Short case presentation. Pierre-Robin sequence.简短病例报告。皮埃尔-罗宾序列征。
Paediatr Respir Rev. 2004 Mar;5(1):90, 92.
7
A genetic follow-up study of 64 patients with the Pierre Robin complex.一项对64例皮埃尔·罗宾综合征患者的基因随访研究。
Am J Med Genet. 1987 Sep;28(1):25-36. doi: 10.1002/ajmg.1320280105.
8
Visual complications of Stickler syndrome in paediatric patients with Robin sequence.患有罗宾序列征的儿科患者中施特勒综合征的视觉并发症。
J Craniomaxillofac Surg. 2007 Mar;35(2):76-80. doi: 10.1016/j.jcms.2007.01.001. Epub 2007 Apr 18.
9
Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.非综合征性腭裂、罗宾序列征和小颌畸形中的胶原蛋白XI序列变异。
Eur J Hum Genet. 2003 Mar;11(3):265-70. doi: 10.1038/sj.ejhg.5200950.
10
Catel-Manzke syndrome: two new patients and a critical review of the literature.卡特-曼兹克综合征：两例新病例及文献综述
Eur J Med Genet. 2008 Sep-Oct;51(5):452-65. doi: 10.1016/j.ejmg.2008.03.005. Epub 2008 Apr 11.
Zotero 插件