Missense mutation - Globe Thesis

Keyword [Missense mutation] Result: 1 - 20 \| Page: 1 of 3
1.	Analysis Of Ps-1, ApoE, And MTHFR Polymorphisms Or Mutations In Patients With Dementia
2.	Missense Mutations And Gene-environment Interaction In Essential Hypertension And Myocardial Infarction Of Japanese Peoples
3.	Idenfication Of The Pathogen By Molecular Biological Methods And Exploration Of Pathogenesis Of The New Entity-Fatal Bacteria Granuloma After Trauma
4.	Establishment And Clinical Application Of The Laboratory Diagnostic Test Of Malignant Hyperthermia
5.	Research On Clinic Presentation And Molecular Biology Of Patients With Adrenoleukodystrophy
6.	Molecular Epidemiology Investigation Of Enlarged Vestibular Aqueduct Associated With SLC26A4 Gene
7.	Incidence And Complete Molecular Characterization Of Glucose-6-phosphate Dehydrogenase (G6PD) Deficiency In Guangxi Zhuang Autonomous Region Of Southern China: Description Of Four Novel Mutations
8.	The Investigation Of The Gene Mutation About Arg810Gly In Patients With Hypertrophic Cardiomyopathy
9.	Study On The Relationship Between Progesterone Receptor Gene Polymorphism,MDR3(Multidrug Resistance 3) Missense Mutation And Intrahepatic Cholestasis Of Pregnancy
10.	Diagnosis Of A Patient With MCD Deficiency By Cytogenetic And Multiple Molecular Genetic Techniques
11.	Investigation Of SLC26A4 Gene In Patients Associated With Sensorineural Hearing Loss In Northwest China
12.	Clinical Features And Molecular Diagnosis Of Hyperimmunoglobulin E Syndrome
13.	A Novel Scn1a Missense Mutation P. Leu193phe Associated With Gefs~+
14.	Herg Missense Mutation A422t And H562p Lead To Cell And Molecular Mechanism Of Lqt Syndrome
15.	Homozygous Embryos With Slc33a1Missense Mutation S113R Showed Early Developmental Arrest
16.	Molecular Genetic Analysis In A Chinese Family With Avellino Corneal Dystrophies
17.	The Sequencing Of KCNJ5Gene In Aldosterone-producing Adenoma In Xinjiang Region
18.	The Study On The Molecular Genetics Of Malignant Hyperthermia In Chinese Pedigrees
19.	Amissense Mutationof The α-galactosidase A Geneina Chinese Familyof Fabry Disease With Renal Failure
20.	The Preliminary Study Of Pathogenesis In Autosomal Dominant Hyper IGE Syndrome With STAT3Mutations
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