Exome - Globe Thesis - Globe Thesis

Keyword [Exome] Result: 61 - 80 \| Page: 4 of 10
61.	The Study Of Human Hepatocellular Carcinomas Revealed By Whole-exome And Transcriptome Sequencing
62.	Exome Sequencing Revealed Novel Germline Mutations In Chinese Peutz-Jeghers Syndrome Patients
63.	Exome Sequencing Identifies Novel Compound Heterozygous Mutations In SPG11That Cause Autosomal Recessive Hereditary Spastic Paraplegia
64.	Mutation Identification Of Pathogenic Gene For Two Families With Limb Malformation
65.	A Study On Whole Exome Sequence Data Analysis And Its Application In Hepatocellular Carcinoma
66.	Capture And Identification Of New Pathogenic Genes In Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
67.	Mutation Screening For An Idiopathic Generalized Epilepsies Pedigree By Exome Sequencing
68.	Diagnosis Of A Recessive Progressive Myoclonic Epilepsy Pedigree By Using Whole Exome Sequencing
69.	Screening For The Causative Gene In An Autosomal Recessive Cerebellar Ataxia Pedigree Using Exome Sequencing
70.	MLPA And Exome Sequencing-Based Molecular Diagnostic Methods For Duchenne/Becker Muscular Dystrophy
71.	A Preliminary Study Of Identifying The Causative Gene Of A Schizophrenia Pedigree
72.	The Identification Of Gene Mutation Profiling In Primary Liver Cancer And The Analysis Of Expression Pattern Of Differentiation-related Genes
73.	Identification And Functional Analysis Of The Pathogenic Gene Of Dyschromatosis Universalis Hereditaria
74.	Searching For The Pathogenic Variant Of A Olmsted Syndrome-like Pedigree By Whole Exome Sequencing
75.	Deep Sequencing Identifies Mutation Genes Related To TCCB And Validation Of The HECW1Mutation
76.	A Pilot Study Of Human Whole-exome Sequencing On Gene Chip For Oral Cancer SNPS
77.	Exome Sequencing Search Causal Gene For Autosomal Dominant Hereditary Hypotrichosis Simplex
78.	Identifying Mutation Genes For Focal Segmental Glomerulosclerosis
79.	Mapping And Identification The Pathogenic Gene In A Family With Nonsyndromic Hereditary Hearing Loss
80.	Whole Exome Sequencing Identifying Genetic Etiology Of Congenital Scoliosis In Chinese Han Population
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