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Keyword [Muscular dystrophy]
Result: 1 - 20 | Page: 1 of 10
1. Genetic Research Of 4q35 In Facioscapulohumeral Muscular Dystrophy(FSHD)
2. The Study Of Clinical Features, Pathology, Emerin And The Expression Of STA Gene In Patients With Emery-Dreifuss Muscular Dystrophy
3. The Experimental And Clinical Study On Diagnosis And Therapy Of Idiopathic Inflammatory Myopathy
4. The Study On The Cellular And Molecular Mechanism Of Cardiomyopathy Associated With Muscular Dystrophy Due To Dystrogycan Deficiency
5. Study Of DMD Gene Deletion Mutation And Using The Junction Fragment For Gene Diagnosis
6. Immunopathological Diagnosis And Molecular Immunopathogenesis Of Idiopathic Inflammatory Myopathies
7. Immunohistochemistry And Western Blotting With Micro-sample In The Diagnosis Of Muscular Dystrophy
8. Deletion / Duplication Mutation Detection Technology Evaluation And Diagnosis Strategies And A Congenital Nystagmus Family Gene Mutation Detection
9. The Clinical And Histopathological Features Of Facioscapulohumeral Muscular Dystrophy (FSHD) And The Study Of Vascular Factors In The Pathogenesis Of FSHD
10. Pathological Gene Screening And The Applicational Study Of Chinese Patients With Neuromuscular Diseases
11. Study On The Molecular Genetics And Gene Diagnosis Of Facioscapulohumeral Muscular Dystrophy In Chinese
12. Detection Of Duchenne Muscular Dystrophy Carrier By Fluorescence Quantitative Polymerase Chain Reaction
13. Studying Distribution Of Dystrophin Gene Deletion In The Northeastern Of China Via Multiplex PCR And Applicating In The Clinical Diagnosis
14. Establishment Of Pulsed Field Gel Electrophoresis System And Study On The Gene Structure Of Facioscapulohumeral Muscular Dystrophy In Chinese Population
15. Use Of Fetal Specific Antbody-HbF(γ Chain) To Detect Fetal Erythroblasts For Non-invasive Prenatal Diagnosis Of DMD
16. Oculopharyngeal Muscular Dystrophy Pathological And Genotypic Studies In The Chinese Population
17. Application Of PCR Technique For The Diagnosis In DMD Patients And Carriers With The Deletion Of Dystrophin Gene
18. Preliminary Study Of A Family With Ophthalmoplegia,Dysphagia And Facial Weakness
19. The Quantitative Study On Muscular Fiber Type In Duchenne Muscular Dystrophy
20. Facioscapulohumeral Muscular Dystrophy In Chinese Population Characteristics Of Alleles 4qA/4qB In 4q Subtelomere
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