Keyword [Whole Exome] Result: 181 - 200 | Page: 10 of 10 181.  The Study Of Clinical Features And Analysis Of Chromosome And Whole Exome Sequencing Of Twins With Biliary Atresia 182.  Genetic Background And Clinical Study Of Children With Congenital Renal Tubular Acidosis 183.  A Clinical Study On Susceptibility Gene Whole Exome Sequencing Of Radiation-Induced Lung Injury In Lung Cancer Patients Treated With Radiotherapy 184.  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 185.  Screening And Identification Of Disease-Causing Gene In A Mental Retardation Family 186.  A Novel Mutation In NRL Gene Causes Autosomal Dominant Retinitis Pigmentosa 187.  Screening Of Pedigrees Of Primary Biliary Cholangitis And Exploration Of Rare Mutations By Whole Exome Sequencing 188.  Whole Exome Sequencing Identifying Causative Gene In A Migraine Without Aura Pedigree 189.  Genetic Exploration Of Bipolar Disorder In Chinese Population Using Whole Exome Sequencing 190.  Allelic Imbalance In Four Tumor Types 191.  Analysis Of Whole Exome Sequencing In 330 Children With Suspected Genetic Diseases 192.  Apatinib In Advanced Gastric Cancer: Efficacy Analysis Based On Real-World Data And Exploratory Study On Inrtinsic Resistance Associated Mutations By Whole-Exome Sequencing 193.  Mutation Screening Of Pathogenic Genes For Premature Ovarian Insufficiency In A Consanguineous Family And A Preliminary Functional Study Of The Novel Homozygous Mutation 194.  Identification And Functional Analysis Of Causative Gene In An Autosomal Recessive Family With Lipid Deposition And Joint Contracture 195.  Primary Renal Synovial Sarcoma:A Case Report,Mutation Landscape And Intra-tumor Heterogeneity Analysis 196.  Verification Experiments In Vitro On Three Likely Causative Genes Of PSIS Obtained From Whole-Exome Sequencing 197.  Mutation Analysis And Pathogenic Gene Localization Of Candidate Genes In A Benign Familial Infantile Epilepsy Family 198.  Differential Diagnosis Of Classical Hodgkin Lymphoma And Anaplastic Large Cell Lymphoma With Aberrant T/B Cell Antigen Expression 199.  Research On The Pathogenic Genes And Related Pathogenic Mechanisms Of Acrokeratoelastoidosis 200.  Analysis Of Chromosomal Aberrations In Fetuses With Heart Defects   <<First  <Prev  Next>  Last>>  Jump to

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