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- Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode. 摘要牙本质形成不良是一种体染色体显性遗传的中胚层缺陷。
- Dentinogenesis imperfecta type I(DGI-I) is an autosomal dominant dental disease with abnormal dentin production and mineralization. 我国科学家成功地克隆了遗传性乳光牙本质I型病的基因,为遗传性乳光牙I型病的诊断带来希望。
- dentinogenesis imperfecta of type Ⅱ 玑牙本质发育不全Ⅱ型
- Dentinogenesis imperfecta Type Ⅱ 牙本质发育不全Ⅱ型
- dentinogenesis imperfecta hereditaria 遗传性牙质生长不全
- Keywords genetic heterogeneity;dentinogenesis imperfecta;linkage analysis; 关键词遗传异质性;牙本质发育不全;连锁分析;
- Keywords Dentinogenesis imperfecta Dentin dysplasia Pedigree Phenotype; 牙本质发育不全;牙本质生成不全;家系;表型;
- The isoionic emission spectrographic analysis of elements in dentinogenesis imperfecta 遗传性乳光牙本质牙体元素成分的分析
- Keywords Dentinogenesis imperfecta Element Isoionic emission spectrographic analysis; 遗传性乳光牙本质;化学元素;等离子体发射光谱分析;
- Keywords Dentinogenesis imperfecta;Linkage(Genetics);Tandem repeat sequences;Chromosomes;human;pair 4; 关键词牙本质生成不全;连锁(遗传学);串联重复序列;染色体;人;4对;
- dentinogenesis imperfecta 牙本质生长不全,牙质生长不全
- Objective To investigate the role of hepatocyte growth factor (HGF) in rat's reparative dentinogenesis. 摘要目的探讨肝细胞生长因子(HGF)在大鼠修复性牙本质形成过程中的作用。
- Objective To evaluate the diagnostic value of X-ray in osteogenesis imperfecta of fetus. 目的评估X线对胎儿期成骨不全的诊断价值。
- Tertiary dentinogenesis is a protective reaction caused by dentin-pulp complex to respond to surrounding pathological stimulus. 第三期牙本质形成是牙髓-牙本质复合体因外界病理性刺激而产生的一种保护性反应。
- Objective To summarize the experience of pamidronate for osteogenesis imperfecta. 目的总结帕米膦酸钠在成骨不全症中的应用经验。
- Methods To review the effect of intravenous pamidronate therapy on two patients with osteogenesis imperfecta in 2007. 方法对2007年我院收治的2例成骨不全症的治疗进行回顾分析。
- AIM: To establish the animal model of re pa rative dentinogenesis and investigate the histo-morphological feature of reparat ive dentinogenesis. 目的:建立修复性牙本质形成的动物实验模型,观察修复性牙本质形成的组织形态学特征。
- The purpose of this study is the concern caregivers issue with regards to strategies and coping with adolescents who have Osteogenesis Imperfecta. 本研究的目的是探讨成骨不全症之青少年及其主要照顾者对疾病在照护过程中所关注的内容及因应的策略。
- Osteogenesis imperfecta is an inherited disorder of connective tissue, which affects the skeleton, ligament, skin, sclera, and dentin. 摘要骨发生不全是一种遗传性的结缔组织病变,常侵犯骨骼、韧带、皮肤、角膜及牙齿。
- We report a 20-year-old male patient with Osteogenesis imperfecta, who suffered from multiple long bone fractures and spinal kyphoscoliosis since his childhood. 本研究报告一例廿岁的男性骨发生不全患者,自幼年起即常发生四肢长骨骨折,并由于脊椎变形严重,造成心肺功能障碍。