Mutation Analysis - Globe Thesis

Keyword [Mutation Analysis] Result: 101 - 120 \| Page: 6 of 10
101.	The Research On Gene Mutation Analysis Of SPG4 And SPG3A In Hereditary Spastic Paraplegia Patients
102.	Mutation Analysis Of GIGYF2 Gene
103.	Localization And Analysis Of Mutation In A Primary Paroxysmal Kinesigenic Dystonia Family
104.	A Novel Locus For Congenital Simple Microphthalmia Families Mapping To 17p12-q12
105.	Detection Of The BCR-ABL Fusion Gene Levels In Chronic Myeloid Leukemia Patients By Real-time Quantitative RT-PCR And Mutation Analysis In The Imatinib Resistant Patients
106.	ATP7B Gene Exon Mutation Analysis In Wilson Disease Children
107.	Mutation Analysis Of Parkin And PINK1 Genes In Early-onset Parkinson'sdisease In China
108.	Mutation Analysis Of FOXL2 Gene In Patients With Blepharophimosis-ptosis-epicanthus Inversus Syndrome (BPES)
109.	Parkin Deletion And Meis1 P. R272H Mutation Analysis Of A Restless Legs Syndrome/Parkinson's Disease Pedigree
110.	Detection Of STK11 Germline Mutation In A Chinese Family With Peutz-Jeghers Syndrome
111.	Mutation Analysis For The Mitochondrial DNA In A Pedigree With Aminoglycoside Antibiotic Induced Deafness
112.	Mutation Analysis For TGFBI Related Corneal Dystrophies
113.	Research On Clinical Features And Mitochondrial DNA Mutation Analysis Of Hereditary Spastic Paraplegia Type 4 (SPG4) Patients
114.	Mutation Analysis Of CITED2 In Patients With Congenital Heart Disease
115.	Analysis On The Gene Mutation Of SCA3 And SCA7 In Two SCAs Families
116.	Study Of Methylation Levels Of The Parkin Gene Promoter And Mutation Analysis Of DJ-1 In Parkinson's Disease Patients
117.	ATP7B Gene Mutation Analysis In The Patients With Wilson Disease
118.	Polyalanine Repeat Expansion Mutation Of The HOXD13 Gene In A Chinese Family With Unusual Clinical Manifestations Of Synpolydactyly
119.	Gene Mutation Analysis In A Kindred With Hereditary Spherocytosis
120.	Mutation Analysis Of The ECM1 Gene In A Chinese Family With Lipoid Proteinosis
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