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Keyword [Exome]
Result: 161 - 180 | Page: 9 of 10
161. A Novel Mutation Of GATA4(K300T)Associated With Familial Atrial Septal Defect
162. Identifying Susceptibility Genes Of Childhood Bronchial Asthma Within 5q31-33 By Exome Sequencing Technology
163. The Establishment Of Icotinib Resistant Non-small Cell Lung Cancer Cell Lines And The Study On Its Genomic Aberrations
164. Pathogenic Gene Research Based On Cases Diagnosed With Isolated Coarctation Of The Aorta
165. Identification Of Disease-Causing Mutations Of Thoracic Aorta Dissection And Abdominal Aorta Aneurysm By Whole Exome Sequencing
166. Exome Sequencing Screen Susceptibility Gene Or Loci Of Systemic Lupus Erythematosus In Yunnan Han Population
167. Whole Exome Sequencing Identifies The Causative Gene Mutation In A Chinese Family With Hereditary Spastic Paraplegias
168. Function Study On The SCRC Candidate Gene DDI2,Based On Whole Exome Sequencing Technology
169. A Series Of Studies On Prenatal Investigation And Diagnosis Of Genetic Etiology With Congenital Cleft Lip And Palate
170. Whole Exome Sequencing And Its Significance Of Idiopathic Generalized Epilepsy With Generalized Tonic-clonic Seizures Only Patients
171. The Research Of Whole-exome Sequencing On Juvenile Myoclonic Epilepsy Patients And Its Clinical Significance
172. Identify Pathogenic Variant For Usher Syndrome By Wholeexome Sequencing
173. Disease Genes Detection Of Two Anterior Segment Abnormalities Pedigree By Whole Exome Sequence
174. Study On A Pedigree Of Inherited Cardiac Conduction Block Through The Whole Exome Sequencing
175. A Novelmutation Of MSX2 Associated With Non-syndromic Cryptorchidism In A Chinese Family By Whole-exome Sequencing
176. Application Of Whole Exome Sequencing In The Study Of Hepatocellular Carcinoma Metastasis
177. Clinical And Pathological Significance And Molecular Identification Of Hepatocellular Carcinoma With Multi-histological Structures
178. Detection Of Whole-exome Region Variations In Breast Cancer Susceptibility Genes BRCA1/2-based On Multiplex PCR-targeting Sequencing
179. Mapping And Cloning Of New Disease-causing Gene In A Autosomal Dominant Optic Disc Pits Family
180. Identifying The Causative Gene Of An Olmsted Syndrome Kindred By Whole Exome Sequencing,and KRT9 Gene Mutation Analysis And Prenatal DNA Diagnosis Of Four Epidermolytic Palmoplantar Keratoderma Pedigrees
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