Mutation Screening - Globe Thesis

Keyword [Mutation Screening] Result: 21 - 40 \| Page: 2 of 6
21.	Mutation Screening Of EXT Genes In A Chinese Hereditary Multiple Exostoses Family
22.	Noncompaction Of Ventricular Myocardium In Patients With Clinical Features, Imaging Characteristics And Candidate Gene Mutation Screening
23.	Mutation Screening And Functional Analysis Of NOTCH1 Gene In Tetralogy Of Fallot
24.	The Genetic Study For Auditory Neuropathy
25.	Study On The Transcriptional Regulation Of Spermatogenesis-related Gene ZNF230 And Mutation Screening Of UBE2B Gene In Patients With Azoospermia
26.	Mutation Screening Of The KCNQ4 And GJB3 Gene In High Frequencies Hearing Loss Population
27.	Linkage Analysis In Two Chinese Family With Congenital Fibrosis Of Extraocular Muscles And Mutation Screening Of Kif21A
28.	Disease Gene Positional Cloning Of Disseminated Superficial Porokeratosis
29.	Preliminary Studies Of Prevalence About Brugada-type Electrocardiogram In Healthy Examination And Mutation Screening Of SCN5A Gene
30.	Molecular Genetic Analysis Of The Mitochondrial DNA 1555 Mutation Gene Among Nonsyndromic Hearing Impairment Patients From Jilin Province
31.	Clinical Analysis And Gene Mutation Screening Of SCN1B And SCN1A In Generalized Epilepsy With Febrile Seizures Plus Families
32.	Establishment And Application Of Mutation Screening System Based On DHPLC For Hereditary Deafness
33.	Clinical Genetic Mechanisms For Auditory Neuropathy
34.	The Mutation Screening And Primary Functional Study On The Cadidate Gene Of Familial Progressive Cardiac Conduction Defect With Long QT Syndrome
35.	Clinical Analysis And Gene Mutation Screening Of SCN1A With Two Hereditary Epileptic Syndromes (GEFS~+ & Dravet Syndrome)
36.	Clinical Analysis Of 15 Cases With Arrhythmogenic Right Ventricular Cardiomyopathy And Mutation Screening Of DSG2 In Patients
37.	The Molecular Aetiology Study In Non-syndromic Hearing Impairment
38.	Mutation Screening In CDS Of LOH12CR1 From Colorectal Carcinoma And Preparation Of Rabbit Antibody Against Human LOH12CR1 Protein
39.	Mutation Screening Of SOX10 Gene In One Chinese Family With Waardenburg Syndrome Type 2
40.	LHX1 Mutation Screening In Patients With Müllerian Duct Abnormalities Of Unknown Cause
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