dentinogenesis imperfecta

Clinical analysis of dentinogenesis imperfecta type ⅱ in a large Mongolian family

蒙古族牙本质发育不全Ⅱ型一大家系临床分析

Pathogenic gene linkage analysis of a family with dentinogenesis imperfecta type II

1个牙本质生长不全Ⅱ型家系疾病基因的连锁分析

Study on the Pathogenic Gene of Dentinogenesis Imperfecta of Type ⅱ

Ⅱ型牙本质发育不全的致病基因研究进展

A Case Report of Dentinogenesis Imperfecta Shields Type ⅱ and Literature Review

遗传性乳光牙本质病例追踪报告

Mutation analysis of disease gene DSPP in dentinogenesis imperfecta Shields type ⅱ

遗传性乳光牙本质致病基因DSPP的突变分析

Objective To map the pathogenic genes of a family with dentinogenesis imperfecta type II to chromosomal position .

目的对一个牙本质生长不全Ⅱ型家系疾病基因进行定位。

Objective To decipher the clinical characteristics and genetic bases of Dentinogenesis imperfecta type II in a large Mongolian family .

目的探明蒙古族一大家系牙本质发育不全症的临床特点和遗传学基础。

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

AIM : To investigate possible gene mutations in DPP coding sequence and DSPP promotor in two Chinese dentinogenesis imperfecta type ⅱ ( DGI - ⅱ) family .

目的：对2个遗传性牙本质发育不全Ⅱ型（DGI-Ⅱ）家系的DSPP启动子和DPP基因编码序列进行突变检测。

Dentinogenesis imperfecta Shields type II ( DGI-II , MIM 125490 ) is an autosomal dominant disorder in which both primary and permanent teeth are affected .

遗传性乳光牙本质（DentinogenesisImperfectatypeⅡ，DGI-Ⅱ）是一种常染色体显性遗传病。