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Keyword [Exome]
Result: 181 - 200 | Page: 10 of 10
181. 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
182. Whole Exome Sequencing Identifiy Novel PRPF31 Mutations In RP And Function Study Of EMC9 Of RP Causitive Gene
183. Mutation Detection Of The Pathogenic Gene In A Pedigree With Reticular Pigmented Anomaly Of The Flexures
184. The Role Of SETD8 In Genome Intergrity Maintenance And Tumoregenesis
185. Primary Sjogren's Syndrome Susceptibility Gene And Preeclampsia Candidate Genes
186. Identification And Functional Analysis Of NEFH Gene In A Pedigree With Charcot-Marie-Tooth Disease
187. Analysis Of Secondary Causes In Fahr's Syndrome And Whole Exome Sequencing In Fahr Disease
188. Genetic Analysis And Pathogenetic Study Of Parkinson's Disease Associated With CHCHD2
189. Mutation Screening And Gene Diagnosis Of Rare Skin Diseases
190. 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
191. Whole Exome Sequencing Identified LncRNAGAS8-AS1 As Papillary Thyroid Carcinoma Suppressor Gene And Its Mechanism Research
192. Exploring Genomic Variants And Genes In Hepatocellular Carcinoma By High-throughput Sequencing Technology
193. The Study On Application Of Combined Genetic Testing Technologies For Laboratory Diagnosis Of Rare Genetic Disease
194. Genomics Investigation Of Gastrin-Independent Gastric Neuroendocrine Neoplasms & Surgical Strategies Of Simultaneous Resection For Synchronous Colorectal Liver Metastases
195. Molecular Researches Of FLNB In Developmental Skeletal Malformations
196. Susceptibility Genes For Nonsyndromic Cleft Lip And Palate In China Detected By Whole Exome Sequencing And Treatment Analysis Of Secondary Deformity Of Nostril Sill
197. Clinical Research And Preliminary Analysis On Genetics Of Congenital Microtia With Thoracic Deformities
198. Preliminary Genetic Analysis And Comprehensive Treatment Of Auriculocondylar Syndrome
199. Phenotype Analysis And Genetic Study Of Chinese Treacher Collins Syndrome Patients
200. Mechanical Properties Measurement,proteomic And Genomic Studies Of Idiopathic Male Infertility On A Chinese Consanguineous Family
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