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Keyword [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. Exome Sequencing In Gene Identification In Recessive Hereditary Hearing Loss And Pheno Type-genotype Correlation
7. Exome Sequencing Identiifes The Pathogenic Gene NCSTN Of Acne Inverse
8. Study On Pathogenesis Of Fanconi Anemia And Its Related Diseases By High - Throughput Analysis Technique
9. Genetic Analysis Of Familial Cryptorchidism By Whole Exome Sequencing
10. Exome Sequencing Identifies TSC22D2 As The Candidate Susceptibility Genes Of Multi-Cancer Pedigree
11. Whole Exome Capture Sequencing Identifies Candidate Genes Related To HCC
12. Exome Sequencing Identifies A Causal Gene Of Disseminated Superficial Actinic Porokeratosis
13. Exome Sequencing Identified Causal Gene COL14A1for Punctate Palmoplantar Keratoderma
14. Exome Sequencing Identified Causal Gene EPS8L3for Marie Unna Hereditary Hypotrichosis
15. Whole-Exome Sequencing In A Chinese Pedigree With Hirschsprung Disease
16. Genetic And Biological Characteristics Of Subclones Isolated From A2780and SKOV3Cell Lines Of Human Ovarian Cancer By Distinct Invasion Capacity
17. Identification Of Candidate Colorectal Cancer Predisposing Gene Variants In Early-onset And Familial Cases Using Whole-exome Sequencing
18. Analysis Of PRRT2Gene Mutation And Genotype-phenotype Correlation In A Cohort Of Paroxysmal Kinesigenic Dyskinesia Cases And Using Exome Sequencing To Indentified The Disease-causing Gene Of Gordon Holmes Syndrome
19. Whole Exome Sequencing To Identify A Novel Mutation In SCN5A Associated With Inherited Cardiac Conduction Disease
20. Whole-exome Sequencing Identifies A Causative Gene Of X-linked Dominant High Myopia And The Establishment Of Human Gene Variant Database-LOVD
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