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Keyword [Whole-exome sequencing]
Result: 181 - 200 | Page: 10 of 10
181. Verification Experiments In Vitro On Three Likely Causative Genes Of PSIS Obtained From Whole-Exome Sequencing
182. Mutation Analysis And Pathogenic Gene Localization Of Candidate Genes In A Benign Familial Infantile Epilepsy Family
183. Differential Diagnosis Of Classical Hodgkin Lymphoma And Anaplastic Large Cell Lymphoma With Aberrant T/B Cell Antigen Expression
184. Research On The Pathogenic Genes And Related Pathogenic Mechanisms Of Acrokeratoelastoidosis
185. Analysis Of Chromosomal Aberrations In Fetuses With Heart Defects
186. Mapping The Pathogenic Gene For A Pedigree With Primary Angle-Closure Glaucoma
187. High-throughput Whole-exome Sequencing Identifies New Genetic Variants Associated With Obesity In Chinese Children And Adolescents
188. Identification Of A Disease-causing Gene In STGD Family And Its Potential Role In Corneal Dystrophy
189. Screen Of Genes Associated With Normal Skull Morphology Of Han Adults In Liaoning Province Based On Whole-exome Sequencing
190. Mutation Of DNA Damage Repair Pathway-related Genes In High-grade Serous Ovarian Cancer By Whole-exome Sequencing
191. Clinical,Genetic And Psychological Features Of Paroxysmal Kinesigenic Dyskinesia
192. The Preliminary Application Of Single Cell Whole Exome Sequencing On Clonal Evolution Of Metastatic Colorectal Cancer
193. Genetic Study Of Hepatic Lipid Metabolism In Hereditary Cholesterol Gallstone Patients
194. Analysis Of Congenital Ptosis Samples By Whole Exome Sequencing
195. A Novel PAX9 Mutation Identification And Functional Verification Of A Patient With Congenital Non-syndromic Hypodontia
196. Etiological Study Of Short Fetal Limbs In The First And Second Trimester And Noninvasive Prenatal Screening Of Fetal Achondroplasia
197. The Research In Causative Genes Of Pediatric Henoch-Schonlein Purpura
198. The Genetic Studies Of Syndromic Craniosynostosis And The Pathogenesis Of Carpenter Syndrome
199. The Screening Of Core Family Affected With Autism Spectrum Disorder Via Whole Exome Sequencing And Effect On Behavior In Early Postnatal Fluoxetine Treated On Zebrafish
200. Screening And Research Of Rare Variants In The Coding Region Of ABCA1 Gene In Patients With Primary Open-angle Glaucoma
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