Font Size: a A A
Keyword [Whole exome sequencing(WES)]
Result: 1 - 19 | Page: 1 of 1
1. Clinical And Molecular Genetics Of Vaginal Septal Syndrome
2. The Role Of C10ORF2 And HELQ,PR1M1 Genes Played In Primary Ovarian Insufficiency
3. Study Of Biomarkers For Molecular Classification In Hepatocellular Carcinoma And Prostate Cancer
4. Molecular Genetic Studies Of Vaginal Oblique Syndrome
5. The Research Of Whole-exome Sequencing On Juvenile Myoclonic Epilepsy Patients And Its Clinical Significance
6. To Distinguish Synchronous Endometrial And Ovarian Endometrioid Carcinoma With Metastatic Cancer By Next-generation Sequencing
7. Clinical Analysis Of Assisted Reproductive Technology With Müllerian Duct Abnormalities Of Assisted Reproductive Technology And Gene Mutation Study
8. Genetic Study Of Hepatic Lipid Metabolism In Hereditary Cholesterol Gallstone Patients
9. A Novel PAX9 Mutation Identification And Functional Verification Of A Patient With Congenital Non-syndromic Hypodontia
10. The Genetic Studies Of Syndromic Craniosynostosis And The Pathogenesis Of Carpenter Syndrome
11. PI3K-Akt Signaling Pathway Involvement In Hemifacial Microsomia By Inhibiting Bone Modeling
12. Genetic Analysis And Literature Review Of 6 Cases Of Hereditary Spherocytosis
13. Mutation Gene Detection And Clinical Phenotype Analysis Of A Family Of VHL Syndrome
14. The Pathogenic Gene Study Of A Family With Hashimoto's Thyroiditis And The Association Analysis Of SNP Rs12532, Rs870142 And The Risk Of Congenital Heart Disease In Tibetans
15. Screening Pathogenic Genes By WES And Investigating The Influence Of RhTPO On Megakaryocytopoiesis And Thrombocytopoiesis In ITP
16. Concurrence Of Myelodysplastic Syndromes And Large Granular Lymphocyte Leukemia:Clinicopathological Features,Mutational Profile And Whole-Exome Sequencing Analysis In A Single Center
17. The Research On Genetic Test And Pregnancy Outcome Of Fetuses With Congenital Anomalies Of The Kidney And Urinary Tract
18. Identification And Integrated Analysis Of Key Genes In Association With Development And Progression Of Adenocarcinoma At The Gastroesophageal Junction In Chinese Population
19. Identification And Gene Therapy Of Pathogenic Genes In Retinitis Pigmentosa
  <<First  <Prev  Next>  Last>>  Jump to