Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.
摘要牙本形成不良是一种体染色体显性遗传的中胚。
Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.
摘要牙本形成不良是一种体染色体显性遗传的中胚。
AIM: To establish the animal model of re pa rative dentinogenesis and investigate the histo-morphological feature of reparat ive dentinogenesis.
目的:建立复性牙本形成的动物实验模型,观察复性牙本形成的组织形态学特征。
AIM: To investigate if there are disease-specific mutations within the dentin phosphoprotein in two dentinogenesis imperfecta type Ⅱfamilies,and analyse the nucleotide polymorphism in DPP region.
目的:检测牙本白基因在牙本发育不全Ⅱ型患者中是否存在突变,并对其序列多态性进行分析。
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