oculoauriculovertebral dysplasia (OAVD)
基本释义:
眼耳脊椎发育不良
网络释义
1)oculoauriculovertebral dysplasia (OAVD),眼耳脊椎发育不良
2)spondyloepiphyseal dysplasia tarda,迟发性脊椎骨骺发育不良
3)X-linked spondyloepiphyseal dysplasia tarda,X-连锁迟发性脊椎骨骺发育不良
4)spondyloepiphyseal dysplasia tarda gene,迟发性脊椎骨骺发育不良基因
5)spondyloepiphyseal dysplasia tarda(SEDL),迟发性脊椎骨髓发育不良(SEDL)
6)Myelodysplasia
[,mai?l?udi'spleizi?],脊髓发育不良
用法和例句
Identification of a novel mutation IVS2-2A→C of SEDL gene in a Chinese family with X-linked spondyloepiphyseal dysplasia tarda;
X-连锁迟发性脊椎骨骺发育不良家系SEDL基因突变研究
X-linked spondyloepiphyseal dysplasia tarda (SEDL) is a rare osteochondrodysplasia caused by the mutation of SEDL gene, which mainly involves vertebral bodies and hips.
X连锁迟发性脊椎骨骺发育不良(spondyloepiphysealdysplasiatarda,SEDL)是一种少见的由SEDL基因突变引起的骨软骨发育障碍性疾病,病变主要累及腰椎和近端承重大关节。
Mutation of acceptor splice site of the SEDL gene in X-linked spondyloepiphyseal dysplasia tarda causes the activation of cryptic splice site;
X-连锁迟发性脊椎骨骺发育不良SEDL基因剪接受体突变导致潜在剪接位点激活(英文)
Mutations of the SEDL Gene in X-linked Spondyloepiphyseal Dysplasia Tarda;
X-连锁迟发性脊椎骨骺发育不良SEDL基因突变研究
Molecular Study of X-linked Spondyloepiphyseal Dysplasia Tarda in a Large Chinese Kindred;
X-连锁迟发性脊椎骨骺发育不良的分子遗传学研究
Study on rapid diagnosis of spondyloepiphyseal dysplasia tarda family
X连锁迟发性脊柱骨骺发育不良快速基因诊断方法的研究
Spondyloepiphyseal dysplasia tarda associated with progressive arthropathy:report of one case
晚发性脊柱骨骺发育不良并进行性关节病1例
The Interaction between Decidual Protein Induced by Progesterone Depp and Sedlin Related to Spondyloepiphyseal Dysplasia Tarda
孕酮诱导的蜕膜蛋白Depp与脊椎骨骺发育不良病蛋白Sedlin的相互作用
Image Diagnosis in Spondyloepiphyseal Dysplasia Tarda with Progressive Arthopathy
晚发型脊柱骨骺发育不良伴进行性骨关节病的影像学诊断
Ultrastructural study on spondyloepiphyseal dysplasia congenita cartilage resulted from COL2A1 gene mutation
COL2A1基因突变致先天性脊柱骨骺发育不良的软骨组织超微结构观察
Progress in studies on molecular genetics of spondyloepiphyseal dysplasia
脊柱骨骺发育不良的分子遗传学研究进展
Mutation of the Cartilage Oligomeric Matrix Protein Gene in Multiple Epiphyseal Dysplasia;
多发性骨骺发育不良患者COMP基因突变的研究
congenital maldevelopment of spine
先天性脊椎发育不全
Objective. To determine whether the length of sternum is correlated with Scheuermann disease pathogenesis.
目的:明确胸骨的长度与脊椎骨骺骨软骨病发病机理的关联。
They were often accompanied by congenital coxa vara, ischium and pubis hypoplasia, spinal bifida or child carpale stunt.
且常伴有先天性髋内翻、坐耻骨发育不全、脊柱裂以及儿童腕骨发育滞迟等。
A similar structure in embryos of higher vertebrates, from which the spinal column develops.
脊索更为高等的脊椎动物胚胎中的类似结构,脊椎骨由此发育
hereditary craniofacial dysostosis
遗传性颅骨面骨发育不良
The effect of immediate stability of goats′ thoracic vertebra after implanting hemiepiphyseal compression staples
胸椎半侧骨骺加压矫形钉固定后对山羊脊柱即时稳定性的影响
The Study of Growth and Development of the Femoral Head Epiphysis among Children Aged at 0-5 Years Old;
0-5岁儿童股骨头骺生长发育研究
Clinical Research on Epiphysis Changes in Avascular Necrosis of Femur Head between Pre- and Post-operation in the Development Dislocation of Hip;
发育性髋脱位股骨头坏死手术治疗前后头骺改变的临床研究
embryonic development of invertebrate
胚胎发育(无脊椎动物)
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