1.
Treatment of styloid process syndrome with extraoral approach styloidectomy in 136 patients
颈外径路茎突截短术治疗茎突综合征136例
2.
Value of 64-slice spiral CT reconstruction technique in diagnosis of styloid process syndrome
64排螺旋CT重建技术在茎突综合征中的诊断价值
3.
Mutation Analysis on the Pathogenic Gene for Van Der Woude Syndrome
范德伍兹综合征致病基因的突变检测
4.
Study on Mutations of FBN1 and TGFBR2 Genes in Marfan Syndrome;
马凡综合征FBN1和TGFBR2基因突变研究
5.
Explorarat in Relations of Budd-Chiari Syndrome to FVLeiden and FⅡG20210A Mutations;
布-加综合征与FVLeiden及FⅡG20210A突变关系的研究
6.
Study on Mutations of FBN1, TGFBR2 and TGFBR1 Genes in Marfan Syndrome;
马凡综合征FBN1、TGFBR2、TGFBR1基因突变研究
7.
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
8.
Study on Genic Mutation in a Patient with Noonan Syndrome
Noonan综合征1例基因突变研究
9.
Analysis of MCP Mutations in 9 Chinese Children with Hemolytic Uremic Syndrome
溶血尿毒综合征患儿MCP基因突变分析
10.
Eya1 gene mutation test in a Goldenhar syndrome pedigree
Goldenhar综合征家系的eya1基因突变检测
11.
Contrast Study of Conservative Treatments for Hypertrophia Symptom of the 5th Transverse Process of Lumbar Vertebra
第5腰椎横突肥大综合征的保守疗法
12.
Mutations of WNK kinases in patients with Gordon syndrome
Gordon综合征患者WNK基因突变研究
13.
Cauda Equina Syndrome Resulting from Lumbar Disc herniation-A reporte of 12 cases
腰椎间盘突出伴马尾神经综合征(附12例报告)
14.
A Family with Brooke-Spiegler Syndrome: Analysis of the Clinical Features and Mutation Detection;
Brooke-Spiegler综合征一家系的临床特点分析和突变检测
15.
The Clinical Research on Acupotomology in Treatment of the Third Lumber Vertebrae Transverse Process Syndrome;
小针刀治疗第三腰椎横突综合征临床疗效观察
16.
Functional Expression of a Novel SCN5A Mutation K317N Identified in a Chinese Brugada Syndrome Family;
中国人Brugada综合征基因突变K317N的功能表达研究
17.
The Research on the Mutation of Coagulation Factor V of Diseased Tissues in Budd-Chiari Syndrome;
布加氏综合征病变组织因子V突变的研究
18.
Two Novel Mutations in Fibrillin-1 Gene from Patients with Marfan Syndrome;
马凡综合征两种新的原纤蛋白-1基因突变