Mutation Analysis - Globe Thesis

Keyword [Mutation Analysis] Result: 141 - 160 \| Page: 8 of 10
141.	Gene Mutation Analysis Of A Special Charcot-Marie-Tooth Disease Family With Type2Diabetes Mellitus
142.	Genetic Testing And Mutation Analysis For The Cochlear Implantation Children And Their Normal Auditory Phenotype Parents
143.	Qingdao, Shandong Cervical Lesions Hpv16 Urr And E6 Gene Mutation Analysis
144.	On The Impact Of Smoking On Male Semen Parameters In Clinical Research And Smoking Male Sperm Genome Methylation Mutation Analysis
145.	Mapping And Mutation Analysis For Hereditary Congenital Cataract Due To The Mutation Of The Gap-junction Protein Gene
146.	Mutation Analysis Of Infectious And Hereditary Diseases Using Next-generation Sequencing
147.	Mutation Analysis Of Inherited Hair Disorders
148.	The Study Of Clinical Features Of Early-onset Parkinson’s Disease And Gene Mutation Analysis Of PARKIN In Uyghur Family With Early-onset Parkinson’s Disease
149.	Establishment And Application Of Diagnostic System For Gene Mutation Analysis Of Hereditary Polycystic Kidney Disease
150.	The Screening And Mutation Analysis Of A Family With Non-syndromic Hearing Loss
151.	Genetic Screening Of Mutation Hot-spots For Subjects With Nonsyndromic Hearing Loss And A Novel MYO7A Gene Mutation Analysis In A Deafness Family
152.	Mutation Analysis Of PAH Gene In Patients With PKU And Prenatal Diagnosis In Han Population From Northern China
153.	Study On BRAF Gene Mutation Analysis And Early Warning Signal Of Hashimoto’s Thyroiditis With Multifocal Papillary Thyroid Carcinoma
154.	NF1 Molecular Characterization And Neurofibromatosis Type 1 Genotype-phenotype Correlations In Chinese Population
155.	BTK Gene Mutation Analysis Of Agammaglobulinemia English
156.	Mutation Screening Of Exons Of Mesoderm Posterior2Gene In Congenital Scoliosis
157.	Mutation Analysis Of Hairy-and-enhancer-of-split-7Gene Exons In Patients With Congenital Scoliosis
158.	Mutation Analysis Of The Presenilin-1Gene In Alzheimer’s Disease Patients And A Preliminary Study Of Expression With Its Initiation Codon Mutation
159.	Genetic Analysis Of Familial Idiopathic Pulmonary Fibrosis
160.	GABRG2Gene Mutation Analysis In The Patient With Complex Febrile Seizure
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