1.
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
2.
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
3.
KCNJ5 Gly387Arg Mutation Responsible for Familial Long QT Syndrome;
KCNJ5基因Gly387Arg突变导致家族性长QT综合征
4.
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
5.
Study of the mechanism of ventricular arrhythmias in the short QT duration syndrome
短QT间期综合征发生室性心律失常机制探讨
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.
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
8.
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
9.
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
10.
Corrected QT interval prolongation and short-term prognosis of acute coronary syndrome with non-ST-elevation
校正QT间期与非ST段抬高急性冠脉综合征短期预后
11.
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
12.
Study on Multiple Selection and Genetic Improvement of Chinese Fir Clones for Growth and Wood Property;
杉木无性系生长与材性综合遗传改良研究
13.
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
14.
Progresses on the genetic study of 22q11 deletion syndrome
22号染色体长臂近端微片段缺失综合征的遗传学研究
15.
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
16.
Molecular Genetic Studies of Brugada Syndrome;
Brugada综合征分子遗传学研究
17.
Genetic Analysis of UGT1A1 Gene in a Family with Gilbert's Syndrome
Gilbert综合征家系UGT1A1基因遗传学分析
18.
Research progress on genetics of the oculo-ariculo-vertebral syndrome
眼-耳-脊柱综合征的遗传学研究进展