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- chondrodystrophia tarda [医] 迟发软骨营养障碍
- Aim study the characteristic of the hemolysin of Edwardsiella tarda. 目的研究迟缓爱德华菌溶血素的特征。
- Abstract: Aim study the characteristic of the hemolysin of Edwardsiella tarda . 文摘:目的研究迟缓爱德华菌溶血素的特征。
- Objective To explore the relationship between X - linked spondyloepiphyseal dysplasia tarda (SEDL) gene escaping X chromosome inactivation( XCI) and SEDL phenotype. 目的探讨X-连锁迟发性脊椎骨骺发育不良(SEDL)基因逃避X染色体失活(XCI)及与临床表型的关系。
- Conclusion there are at least two kinds of hemolysins of Edwardsiella tarda, activity of which is different with circumstance changing. 结论迟缓爱德华菌至少存在两种溶血素，其溶血活性受环境影响表现不同。
- Isolation and identification showed that the ascites of flounder (Paralichthys olivaceus) were infected only by Edwardsiella tarda, a pathogenic bacteria. 摘要描述了牙鲆腹水病的症状，经对细菌的分离与鉴定表明所检病例均为迟钝爱德华氏菌的单独感染。
- IntroductionX-linked spondyloepiphyseal dysplasia tarda(SEDL, OMIM 313400) is a rare, X-linked recessive osteochondrodysplasia with an estimated prevalence of ~ 1.7 per million in Britain. X-连锁迟发性脊椎骨骺发育不良(X-linked spondyloepiphyseal dysplasia tarda,SEDL,OMIM 313400)是一种罕见的遗传性骨软骨发育不良性疾病。
- congenital calcification chondrodystrophia 先天性钙化性软骨营养不良症
- chondrodystrophia calcificans congenita 亨纳曼(氏)综合征
- chondrodystrophia congenita punctata 点状骨骺发育不良
- chondrodystrophia deformans hereditaria [医] 遗传变形性软骨营养障碍
- chondrodystrophia fetalis calcificans 胎儿钙化性软骨营养障碍, 康拉迪综合征
- chondrodystrophia foetalis cakifican 胎儿钙化软骨养障碍
- Distribution and Actuality of Otis tarda in China 中国鸨类的分布与现状
- sclerodermoid porphyria cutanea tarda 硬皮病样迟发性皮肤卟啉症
- porphyria cutanea tarda hereditaria 遗传性原粪卟啉症
- Porphyria cutanea tarda symptomatica 皮肤迟发性症状性卟啉症
- hereditary porphyria cutanea tarda 遗传性迟发性皮肤卟啉症
- hereditary porphyria cutarea tarda 遗传性迟发性皮肤卟啉病
- Homozygous porphyria cutanea tarda 纯合子性迟发性卟啉症皮肤
