Disease-causing - Globe Thesis

Keyword [Disease-causing] Result: 21 - 40 \| Page: 2 of 3
21.	Investigation On The Disease-causing Gene And Molecular Mechanism For A Hereditary Dentin Dysplasia Type Ⅰ Family
22.	The Negative Regulatory Mechanism Study Of ISG15 On Autoinflammatory Disease
23.	Surgical Treatment Of Hypertrophic Cardiomyopathy And Rare Disease-causing Genes
24.	Using The MiRNA To Discover Genes Associated With Disease
25.	Analysis Of Mutations Of Disease-causing Gene In Sporadic Retinitis Pigmentosa Using Exon Trapping
26.	Detect The Disease-causing Genes And Clinical Analysis Of A Autosomal Dominant Vitreoretinochoroidopathy Pedigree
27.	Research On The Clinical Characteristics And Disease-causing Mechanisms In A Chinese Family With Cleidocranial Dysplasia
28.	Identification Of Disease-Causing Mutations Of Thoracic Aorta Dissection And Abdominal Aorta Aneurysm By Whole Exome Sequencing
29.	Mapping And Cloning Of New Disease-causing Gene In A Autosomal Dominant Optic Disc Pits Family
30.	Swarm Intelligence Optimization Algorithms And Their Application To Association Study Of Complex Diseases
31.	Identification And Molecular Consequence Of A Disease Causing Gene In An Autosomal Dominant Congenital Cataract Family
32.	Diagnosis And Treatment Of Hypertrophic Osteoarthropathy And Mendelian Randomization Study Between 25OHD And Bone Metabolism
33.	An Identification Of The Disease-causing Genes Of A Hereditary Ataxia Family
34.	Screening And Identification Of Disease-Causing Gene In A Mental Retardation Family
35.	Identification Of A Disease-causing Gene In STGD Family And Its Potential Role In Corneal Dystrophy
36.	Pathogenic Mechanism Of Disease-causing Mutation In RYR2 In Catecholaminergic Polymorphous Ventricular Tachycardia
37.	Study Of Novel Disease-causing Gene And Molecular Mechanisms For Charcot-marie-tooth Disease
38.	Social Capital And Influence Of Health Service Utilization In Disease-causing Poverty Population
39.	Disease-causing Gene Screening And Reproductive Intervention For Duchenne Muscular Dystrophy
40.	Characterization of the N-terminal domains and disease-causing mutations of the human Wilson protein
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