1.
DMD gene defection analysis in 135 patients with Duchenne muscular dystrophy
135例Duchenne型肌营养不良症DMD基因缺失分析
2.
Study of DMD Gene Deletion Mutation and Using the Junction Fragment for Gene Diagnosis
DMD基因缺失突变及连接片段应用于基因诊断的研究
3.
Foundational and clinical researches on DNA microarray technique to DMD gene deletions detection;
DNA微阵列技术对DMD基因缺失检测的基础与临床研究
4.
The Relative Research between Gene Deletion with DMD and Carrier Screening;
基因缺失与DMD的关系研究及携带者筛查
5.
Detection of Duchenne/Becker muscular dystrophy gene deletions with multiplex-PCR.
多重聚合酶链反应检测DMD/BMD患者的基因缺失
6.
Application of PCR Technique for the Diagnosis in DMD Patients and Carriers with the Deletion of Dystrophin Gene;
PCR技术在缺失型DMD患者及携带者诊断中的应用研究
7.
Use of Fetal Specific Antbody-HbF(γ Chain) to Detect Fetal Erythroblasts for Non-invasive Prenatal Diagnosis of DMD;
应用胎儿特异性抗体HbF（γ链）标记法无创性产前基因诊断DMD
8.
MLPA Coupled with DHPLC for Rapid Mutation Detection of the Causative Gene in DMD;
联合运用MLPA和DHPLC技术快速检测DMD致病基因的突变
9.
Construction of Goatpox Virus Gene Deleted Transfer Vector and Generation of Gene Deleted Mutant;
山羊痘病毒基因缺失转移载体及基因缺失突变毒株的构建
10.
Study on Pseudorabies Virus Gene-deleted Vaccine, SA215 Strain;
伪狂犬病基因缺失疫苗SA215研究
11.
Analysis of Ocular Phenotype in CYP1B1-null Mice;
CYP1B1基因缺失小鼠眼部表型分析
12.
Clinical Study on Parkin Gene Deletion Mutations in Chinese Patients with Parkinson s Disease;
帕金森病Parkin基因缺失突变的临床研究
13.
Pattern of Insertion and Deletion in Mammalian Genome;
哺乳动物基因组插入、缺失的模式研究
14.
An Analysis of HCCS1 Gene Mutation and Loss of Hetrozygosity in Hepatocellular Carcinoma
肝细胞癌HCCS1基因突变和杂合缺失分析
15.
Deletion of gr/gr-DAZ1/DAZ2 gene and male infertility
gr/gr-DAZ1/DAZ2基因缺失与男性不育
16.
Multiplex PCR genotyping method for human UGT2B17 gene deletion
人类UGT2B17基因缺失的多重PCR分型方法
17.
Prokaryotic Expression of PRRSV dNsp2(87) Gene
PRRSV基因缺失片段dNsp2(87)的原核表达
18.
Correlation Between Loss of p16 Gene and Prognosis in Nasopharnygeal Carcinoma
p16基因缺失与鼻咽癌预后的相关性