Whole-exome sequencing - Globe Thesis

Keyword [Whole-exome sequencing] Result: 161 - 180 \| Page: 9 of 10
161.	X-linked Parkinsonism Caused By A Novel Mutation Of RAB39B: Genetic Analysis And Mechanism Study
162.	Whole Exome Sequencing Analysis And The Establishment Of Imatinib Resistance Cells Of GIST
163.	Two Gene Mutations In MEN1 Founded By Exome Gene Sequencing Causing Sporadic Insulinomas
164.	Whole Exome Sequencing For Pathogenic Genes In A Hypodontia And Tumor-prone Family
165.	Part1.Genomic Sequencing Of Hashimoto Thyroiditis Coexistent With Thyroid Carcinoma Part2.Data Mining Of Esophageal Squamous Cell Carcinoma From The Cancer Genome Atlas Database
166.	Preliminary Identification Of Causative Gene For Tuberous Sclerosis Complex
167.	Evaluation Of Dual Endometrial And Ovarian Carcinomas Based On Next-generation Sequencing And Clinical Pathology Scores
168.	The Study Of Clinical Features And Analysis Of Chromosome And Whole Exome Sequencing Of Twins With Biliary Atresia
169.	A Clinical Study On Susceptibility Gene Whole Exome Sequencing Of Radiation-Induced Lung Injury In Lung Cancer Patients Treated With Radiotherapy
170.	Study On Genomic Evolution Of Rectal Cancer Under Chemoradiotherapy And Genetic Variations Associated With Sensitivity And Survival In Rectal Cancer Patients Of Locally Advanced Rectal Cancer Receiving Preoperative Chemoradiotherapy
171.	Screening And Identification Of Disease-Causing Gene In A Mental Retardation Family
172.	A Novel Mutation In NRL Gene Causes Autosomal Dominant Retinitis Pigmentosa
173.	Screening Of Pedigrees Of Primary Biliary Cholangitis And Exploration Of Rare Mutations By Whole Exome Sequencing
174.	Whole Exome Sequencing Identifying Causative Gene In A Migraine Without Aura Pedigree
175.	Genetic Exploration Of Bipolar Disorder In Chinese Population Using Whole Exome Sequencing
176.	Allelic Imbalance In Four Tumor Types
177.	Analysis Of Whole Exome Sequencing In 330 Children With Suspected Genetic Diseases
178.	Apatinib In Advanced Gastric Cancer: Efficacy Analysis Based On Real-World Data And Exploratory Study On Inrtinsic Resistance Associated Mutations By Whole-Exome Sequencing
179.	Mutation Screening Of Pathogenic Genes For Premature Ovarian Insufficiency In A Consanguineous Family And A Preliminary Functional Study Of The Novel Homozygous Mutation
180.	Identification And Functional Analysis Of Causative Gene In An Autosomal Recessive Family With Lipid Deposition And Joint Contracture
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