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Keyword [Whole Exome]
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1. Study On Full Exon Sequencing Of Focal Nodular Hyperplasia Of Liver
2. Sequencing Of All Exon Groups In Lymph Node Metastasis Of Papillary Thyroid Carcinoma
3. Screening And Functional Study Of Gene Mutations In Nodular Sclerosis And Pyogenic Sweatadenitis
4. Clinical And Molecular Genetics Of Vaginal Septal Syndrome
5. Genetic Susceptibility Of Children 's Still' S Disease And The Administration Of Pearl Monoclonal Antibody
6. Study On Pathogenesis Of Fanconi Anemia And Its Related Diseases By High - Throughput Analysis Technique
7. Genetic Analysis Of Familial Cryptorchidism By Whole Exome Sequencing
8. Whole Exome Capture Sequencing Identifies Candidate Genes Related To HCC
9. Whole-Exome Sequencing In A Chinese Pedigree With Hirschsprung Disease
10. Identification Of Candidate Colorectal Cancer Predisposing Gene Variants In Early-onset And Familial Cases Using Whole-exome Sequencing
11. Whole Exome Sequencing To Identify A Novel Mutation In SCN5A Associated With Inherited Cardiac Conduction Disease
12. Whole-exome Sequencing Identifies A Causative Gene Of X-linked Dominant High Myopia And The Establishment Of Human Gene Variant Database-LOVD
13. Characterization Of Molecular Defects For Genetic Skeletal Disorders By Whole Exome Sequencing
14. The Clinical, Pathological And Genetic Characteristics Of Oculopharyngeal Myopathy Syndrome
15. The Role Of DNA Repair Related Genes CSB-PGBD3, MSH5 And FMR1 Played In Premature Ovarian Failure
16. Study On Factors Related To The Clinical Feature And Molecular Biology Of Hemorrhagic Moyamoya Disease
17. Identification Of Driver Genes In Esophageal Cancer By Whole Genome Sequencing And Whole Exome Sequencing And Functional Validation Of These Genes
18. Hearing Conditions Of Centenarians And Analysis Of Causal Gene In A Chinese Hereditary Hearing Loss Pedigree
19. Identification Of Susceptible Genes And Disease-causing Mutations Of Aorta Diseases
20. The Study Of Mechanism On ETV6/RUNX1 Positive Childhood B-precursor Acute Lymphobalstic Leukemia
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