1.
Gene Mapping of a Hereditary Hypotrichosis Simplex Family;
一遗传性单纯少毛症家系的基因定位
2.
hereditary hemorrhagic telangiectasia
遗传性出血性毛细血管扩张症
3.
A Study of Juvenile s Simplicial Adiposity and Their Sports Activities;
少年儿童单纯性肥胖症与运动的研究
4.
Gene Mutations in Psoriasis and Marie Unna Hereditary Hypotrichosis
银屑病及Marie Unna遗传性稀毛症的遗传易感基因
5.
Mutation Analysis of ALK1 Gene in a Chinese Family with Hereditary Hemorrhagic Telangiectasis Type Ⅱ;
遗传性出血性毛细血管扩张症ALK1基因突变研究
6.
Location and Identification of Human Idiopathic Congenital Talipes Equinovarus Susceptibility Genes;
单纯性马蹄内翻足遗传易感基因的定位与鉴定
7.
pure gonadal dysgenesis
单纯性性腺发育障碍症
8.
simple affective depression
单纯性情感性抑郁症
9.
Pro 275 Ser Homozygous Mutation of PROC Gene Causes Type Ⅱ Inherited Protein C Deficiency
Pro 275 Ser纯合突变导致的Ⅱ型遗传性蛋白C缺陷症
10.
Determination of Mutations in ALK-1 Gene in Chinese Family with Hereditary Hemorrhagic Telangiectasia Disease;
一个遗传性出血性毛细血管扩张症家系ALK-1基因突变检测
11.
Examination techniques and imaging findings in patients with hereditary hemorrhagic telangiectasia
遗传性出血性毛细血管扩张症的检查方法和影像学表现
12.
Color Doppler ultrasound in diagnosis of hereditary hemorrhagic telangiectasia with hepatic involvement
彩超诊断累及肝脏的遗传性出血性毛细血管扩张症
13.
Effect of Exercise on Cerebral Hemodynamics of Simple Obese Children and Adolescent;
运动对少儿单纯性肥胖症脑血液动力学影响的研究进展
14.
Clinical Observation on Children Simple Obesity Treated by Tuina Therapy on Meridians and Acupoints
经络点穴推拿治疗青少年单纯性肥胖症的临床疗效观察
15.
Genetic polymorphism of glutathione s-transferase associated with childhood infectious mononucleosis
儿童传染性单核细胞增多症患者GST基因遗传多态性的研究
16.
Mutation Analysis and Functional Study of U2HR in Chinese Patients with Marie Unna Hereditary Hypotrichosis
Marie Unna型遗传性稀毛症致病基因突变筛查及功能研究
17.
Congenital Generalized Hypertrichosis Terminalis: Genetic Mapping and Pathogenic Mutation Identification
先天性全身终毛增多症的遗传学定位和致病突变研究
18.
Location and Identification of Human Simple Congenital Heart Disease Susceptibility Genes;
人类单纯性先天性心脏病遗传易感基因的定位与鉴定