1.
Molecular Genetic Analysis of Waardenburg Syndrome and Non-syndromic Hearing Loss
Waardenburg综合征和非综合征型耳聋的分子遗传学研究
2.
Clinical Characteristics of No-syndronmic Oligodontia;
非综合征型少牙畸形的临床特征分析
3.
The Comparative Research of Craniofacial Structural Characteristic of Syndromic and Nonsyndromic Patients with Cleft Palate;
综合征与非综合征型腭裂颅颌面结构特征的对比研究
4.
Genome-Wide Scanning for a Nonsyndromic Autosomal Dominant Postaxial Polydactyly in a Six-Generation Family;
非综合征型轴后多指（趾）畸形全基因组扫描分析
5.
Molecular Genetic Analysis of the Mitochondrial DNA 1555 Mutation Gene among Nonsyndromic Hearing Impairment Patients from Jilin Province;
吉林省非综合征型耳聋分子病因学分析
6.
Molecular Finding in Two Chinese Families with Nonsyndromic Hearing Impairment;
两个非综合征型耳聋家系的分子遗传学研究
7.
A meta-analysis of whole-genome linkage scans for non-syndromic cleft lip with or without cleft palate
非综合征型唇腭裂全基因组连锁研究的Meta分析
8.
Mutation analysis of GJB2 gene in deaf population from Chongqing city
重庆市非综合征型耳聋患儿GJB2基因突变分析
9.
Molecular genetic analysis of the mtDNA A1555G mutation in patients with non-syndromic hearing loss
非综合征型耳聋线粒体基因A1555G突变分析
10.
Study on the mode of inheritance of nonsyndromic cleft Lip and/or palates
非综合征型唇裂伴或不伴腭裂的遗传方式
11.
Study on the Mitochondrial DNA Mutation and the Phenotype Diversity of Nonsyndromic Hearing Loss;
非综合征型耳聋线粒体DNA突变及其临床表型多样性的研究
12.
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
13.
Fine Mapping of a Novel Non-Syndromic Postaxial Polydactyly Locus and Critical Region Analysis;
非综合征型轴后多指（趾）家系相关基因的精细定位及关键区域分析
14.
Mutation Screening and Whole Spectrum Mutation Map Drawing of GJB2 Gene among Non-syndromic Hearing Impairment Patients;
非综合征型耳聋患者GJB2基因突变筛查和全频谱突变图谱绘制
15.
Mapping and Postional Cloning the Causative Genes in Chinese Pedigrees with Non-syndromic Hereditary Hearing Impairment;
非综合征型遗传性听力损失家系致病基因定位克隆研究
16.
Clinical and Molecular Genetic Studies in a Chinese Family with Nonsyndromic Oligodontia;
一个非综合征型少牙畸形家系的临床及分子遗传学分析
17.
Association Studies on Susceptibility Loci (Gene) of Two Types of Non-syndromic Hearing Impairment;
遗传性非综合征型耳聋两种致病基因易感位点的关联分析
18.
Zollinger-Ellison syndrome
混合型非胰岛细胞分泌腺瘤;卓艾二氏综合征