1.
Haplotype and linkage analysis in Chinese hereditary mixed polyposis syndrome
华人遗传性混合息肉病综合征患者单倍型及遗传连锁分析
2.
The Study of Molecular Pathogenesis of Fragile X Syndrome;
遗传性智障脆性X综合征发病分子机制研究
3.
One Family Report of Fulfilling Chinese HNPCC Criteria;
符合中国人遗传性非息肉病性大肠癌家系标准的一家系报告附文献综述
4.
Genetic Disorders of Cholesterol Biosynthesis-Pathophysiological Studies of Smith-Lemli-Opitz Syndrome;
遗传性胆固醇合成缺陷性疾病的病理生理研究—史—伦—奥三氏综合征
5.
Genetic Analysis of Non-syndromic Hearing Loss and Waardenburg Syndrome;
非综合征性耳聋及Waardenburg综合征的遗传学分析
6.
Alport's syndrome
遗传性肾炎神经性耳聋综合征;阿尔波特氏综合
7.
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
8.
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
9.
Mapping and Identified the Causative Genes in Chinese Nonsyndromic X-linked Hereditary Hearing Loss Pedigrees;
非综合征型X连锁显性遗传耳聋家系致病基因的定位及鉴定研究
10.
A Genetic Epidemiology Study of Polycystic Ovary Syndrome of Chinese Han Ethnic Women in Guangdong Province
粤籍汉族多囊卵巢综合征遗传流行病学研究
11.
Molecualr Genetics of Klippel-Trenaunay Syndrome and Long QT Syndrome;
先天性静脉畸形骨肥大综合征和长QT综合征的分子遗传学研究
12.
Clinical Analysis and Molecular Genetic Study of Hereditary Nonpolyposis Colorectal Cancer Kindreds;
遗传性非息肉病性大肠癌（HNPCC）家系研究
13.
Characterization of Genotype-phenotype and Clinico-pathological Features in Chinese Hereditary Nonpolyposis Colorectal Cancer Families;
中国人遗传性非息肉病性结直肠癌家系收集、整理及分子遗传学和临床病理特征分析
14.
Clinicopathological and Molecular Genetic Study of Chinese Hereditary Nonpolyposis Colorectal Cancer (HNPCC)
中国人遗传性非息肉病性结直肠癌（HNPCC）临床病理特征及分子遗传学研究
15.
Molecular Mechanism and Functional Characterization Associate with Maternally Inherited Aminoglycoside-induced and Nonsyndromic Deafness;
母系遗传药物性聋与非综合征性聋的分子遗传机制与功能研究
16.
Report of a family with Alport syndrome;
遗传性肾炎研究现状附A1port综合征一家系报告
17.
Three novel mutations of potassium channel HERG and SCN5A in Chinese families of congenital long QT syndromes
遗传性长QT综合征HERG基因及SCN5A基因新突变
18.
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