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Keyword [Exome]
Result: 21 - 40 | Page: 2 of 10
21. Study Of A Novel And Potential Susceptibility Gene To Crohn’s Disease In A Chinese Family By Exome Sequencing And Bioinformatics Methods
22. Identification And Functional Validation Of The Novel Mutated Gene In Human Hepatocellular Carcinoma
23. Characterization Of Molecular Defects For Genetic Skeletal Disorders By Whole Exome Sequencing
24. Familiar Hypercholesterole Candidate Gene Identification Using Exome Sequencing And A Study Of SNP Filtering
25. Application Of Genome-Wide Association Study In Mapping Of Susceptibility Genes In High Myopia And Exome Sequencing In Identifying Genes Responsible For Transposition Of Great Arteries
26. Mutation Analysis Of Infectious And Hereditary Diseases Using Next-generation Sequencing
27. Analysis Of Candidate Susceptibility Genes And Causative Mutation In Autoimmune Diseases
28. Identification And Functional Characterization Of The Disease-causing Mutation Of A Family With Nance-Horan Syndrome
29. The Clinical, Pathological And Genetic Characteristics Of Oculopharyngeal Myopathy Syndrome
30. The Role Of DNA Repair Related Genes CSB-PGBD3, MSH5 And FMR1 Played In Premature Ovarian Failure
31. Study On Factors Related To The Clinical Feature And Molecular Biology Of Hemorrhagic Moyamoya Disease
32. Exome Sequencing Identified Mutation Shift During Neoadjuvant Chemotherapy In Breast Cancer
33. The Clinical And Genetic Analysis Of Multiple Endocrine Neoplasia Type 2
34. Identification Of Driver Genes In Esophageal Cancer By Whole Genome Sequencing And Whole Exome Sequencing And Functional Validation Of These Genes
35. Hearing Conditions Of Centenarians And Analysis Of Causal Gene In A Chinese Hereditary Hearing Loss Pedigree
36. Identification By Exome Sequencing Of The Pathogenic Genes And Analysis Of POFUT1 Gene Mutation Of Dowling-Degos Disease
37. Identifying The Rare Variations In A Chinese Sporadic Congenital Heart Disease Cohort
38. Identification Of Susceptible Genes And Disease-causing Mutations Of Aorta Diseases
39. The Study Of Mechanism On ETV6/RUNX1 Positive Childhood B-precursor Acute Lymphobalstic Leukemia
40. Association Analyses Identifies Psoriasis Insertion/Deletion Variants In Chinese Han Population
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