1.
Muscle segment homeobox gene-1 and non-syndromic hypodontia
同源异型盒基因-1与非综合征型多数牙先天性缺失
2.
A clinical and laboratory study on a case of hypohidrotic ectodermal dysplasia(HED) accompanied by oligodontia
HED伴多数牙先天缺失1例的临床研究
3.
Conclusion Severe tooth agenesis will affect the development of mandible and maxillary bones.
结论多数牙齿先天性缺失会影响上下颌骨的发育。
4.
The Study on Pathogenic Genes PAX9 and MSX1 Related with Oligodontia;
多数牙先天缺失致病相关基因PAX9、MSX1的研究
5.
The detection of MSX1 gene mutations in patients with oligodontia
多数牙先天缺失可能与MSX1上的3个SNPs相关
6.
Treatment experience of 14 cases of congenitally missing second premolar
第二双尖牙先天缺失14例治疗体会
7.
Dentofacial Morphologic Analysis for the Patients with Congenital Absence of Lower Incisor in Jinan;
济南地区下切牙先天缺失患者牙颌面形态研究
8.
congenital absence of endometrium
先天性子宫内膜缺失
9.
congenital absence of organ of Corti
先天性柯替氏器缺失
10.
congenital defects, blindness, etc
先天性缺陷、 失明等.
11.
Study on the Relationship between 22q11 Microdeletion and Simple Congenital Heart Disease;
单纯性先天性心脏病22q11微缺失的研究
12.
The Effect of Tooth Agenesis on Craniofacial Structure;
青少年先天性缺牙对颅颌面发育的影响
13.
The treatment combining orthodontics with implant prosthodontics for cases of the missing mandibular insiors with malocclusion
正畸与种植体联合治疗下前牙先天缺失伴错畸形15例分析
14.
Congenital absence of most of the brain and spinal cord.
无脑畸形大部分大脑和脊髓先天性缺失
15.
Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation-dependent probe amplification
多重连接探针扩增技术在先天性心脏病22q11微缺失/微重复综合征诊断中的应用
16.
Analysis of clinical features and mutation associated with oligodontia
一个单纯性先天缺牙家系的临床及基因突变分析
17.
inborn error of amino acid metabolism
先天性氨基酸代谢缺陷
18.
congenital agammaglobulinemia
先天性血γ－球蛋白缺乏