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Keyword [Whole-exome sequencing]
Result: 101 - 120 | Page: 6 of 10
101. The Study Of Medical Relavent Findings Of 42 Healthy Individuals Using Whole Exome Sequencing And An Intronic Mutation C.6430-3C>G In The F8 Gene Causes Hemophilia A
102. Whole Exome Sequencing Identifiy Novel PRPF31 Mutations In RP And Function Study Of EMC9 Of RP Causitive Gene
103. The Role Of SETD8 In Genome Intergrity Maintenance And Tumoregenesis
104. Identification And Functional Analysis Of NEFH Gene In A Pedigree With Charcot-Marie-Tooth Disease
105. Analysis Of Secondary Causes In Fahr's Syndrome And Whole Exome Sequencing In Fahr Disease
106. Mutation Screening And Gene Diagnosis Of Rare Skin Diseases
107. Involvement Of VPS4B A Dentin Defects ?Causing Gene In The Pathogenesis Of Cognitive Impairments In Vps4b Knockout Mice Study On An Missense Mutation In AMBN Gene Causes Amelogenesis Imperfecta And Dentin Disorders
108. Whole Exome Sequencing Identified LncRNAGAS8-AS1 As Papillary Thyroid Carcinoma Suppressor Gene And Its Mechanism Research
109. Exploring Genomic Variants And Genes In Hepatocellular Carcinoma By High-throughput Sequencing Technology
110. Genomics Investigation Of Gastrin-Independent Gastric Neuroendocrine Neoplasms & Surgical Strategies Of Simultaneous Resection For Synchronous Colorectal Liver Metastases
111. Molecular Researches Of FLNB In Developmental Skeletal Malformations
112. Susceptibility Genes For Nonsyndromic Cleft Lip And Palate In China Detected By Whole Exome Sequencing And Treatment Analysis Of Secondary Deformity Of Nostril Sill
113. Clinical Research And Preliminary Analysis On Genetics Of Congenital Microtia With Thoracic Deformities
114. Preliminary Genetic Analysis And Comprehensive Treatment Of Auriculocondylar Syndrome
115. Phenotype Analysis And Genetic Study Of Chinese Treacher Collins Syndrome Patients
116. Mechanical Properties Measurement,proteomic And Genomic Studies Of Idiopathic Male Infertility On A Chinese Consanguineous Family
117. Whole Exome Sequencing Identifies Pathogenic Genes Of Two Mendelian Genetic Disease Pedigrees And Function Characterization
118. Association Of Single-nucleotide Polymorphisms From The Genes That Regulation Of MiRNA Maturation With Tuberculosis Susceptibility
119. Molecular Genetic Study Of Embryonic (Fetal) Arrest In Early Pregnancy
120. The Research Of New Mutations In Different Phenotypes Of Pediatric Epilepsy Patients
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