Mutation Analysis - Globe Thesis

Keyword [Mutation Analysis] Result: 161 - 180 \| Page: 9 of 10
161.	The Mutation Analysis Of GJB3and GJB4Gene In A Family With Erythrakeratodermia Variabilis
162.	Mutation Analysis Of LMNA Gene For Hutchinson-Gilford Progeria Syndrome And Dilated Cardiomyopathy
163.	Diagnosis Of Patients With Tuberous Sclerosis Complex By Direct Sequencing And MLPA
164.	Clinical, Pathological And Molecular Biological Study On Multiple Acyl-CoA Dehydrogenase Deficiency
165.	Mutation Analysis Of Parkin Gene In Sporadic Early-onset Parkinson’s Disease And Clinical Characteristics Discussion
166.	Gene Mutation Detection Of PMP22, CX32, MFN2in CMT And The Functional Research Of CX32Protein
167.	Mutation Analysis In330Chinese Cases With DMD/BMD And Genetic Analysis In A Fetus With Compound Heterozygous DMD Mutations
168.	Biosensor Amplifying Technique Research Based On Nucleic Acid Probe Conformational Switch
169.	Mutation Analysis Of The Predisposing Gene SORBS2of Non-syndromic Congenital Heart Disease By Denaturing High-performance Liquid Chromatography
170.	Analysis Of Disease Gene Mutation And Function In A Patient With Axenfeld-Rieger Syndrome
171.	Wisp3 Gene Polymorphisms Associated With Postmenopausal Osteoporosis Research Late-onset Spine Epiphyseal Dysplasia Associated With Progressive Joint Department Of A Patient And His Family Wisp3 Gene Mutation Analysis
172.	33 Cases Peja Mei Disease Plp1 Mutation Analysis And 5 Cases Of Prenatal Diagnosis
173.	Mutation Analysis Of The ABCD1Gene In Patients With X-linked Adrenoleukodystrophy And Expression Of ALDP Mutants In Eukaryotic Cells
174.	Clinical Manifestation, Imaging Characteristics, And Gen Mutation Analysis Of One Pedigree Of The Spinocerebellar Ataxia With Severe Cataract
175.	Ciinicai Phenotypes And Gene Mutation Analysis Of Duchenne/Bccker Muscular Dystrophy
176.	A Pathological And Morphological Observation Of Gastric Carcinoma With Neuroendocrine Features And Mutation Analysis Of Sox2Gene
177.	Clinical And Mutation Analysis Of Four Chinese Families With Von Hippel-Lindau Disease
178.	Clinical And Immunological Characteristics, Mutation Analysis Of Two Patients With Omenn Syndrome
179.	Mutation Analysis Of The TSC1and TSC2Genes In Chinese Patients With Tuberous Sclerosis Complex
180.	Mutation Analysis Of ECFR&K-RAS By Realtime Polymerase Chain Reaction Using Scorpion Amplification Refractory Mutation System And Relationship Between EGFR&K-RAS Mutation And Response To Tyrosine Kinase Inhibitor Treatment In Chinese Patients With Non-sma
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