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Keyword [Exome]
Result: 41 - 60 | Page: 3 of 10
41. The Role Of C10ORF2 And HELQ,PR1M1 Genes Played In Primary Ovarian Insufficiency
42. Analysis Of Early-onset Colorectal Carcinoma With Paired Liver Metastases Using Exome Sequencing
43. Molecular Genetics Analysis Of Xeroderma Pigmentosum And Hereditary Gingival Fibromatosis
44. The Research Of The Molecular Disease Mechanism Of Arrhythmogenic Right Ventricular Cardiomyopathy
45. Genetic Research Of Notch Signal Pathway And Congenital Scoliosis
46. Effects Of Cell Division Cycle Associated 2 And Its Mechanism Research In Pancreatic Ductal Adenocarcinoma
47. A Study On Gene Mutations And Related Pathogenic Mechanism Of Hereditary Pigmentary Skin Disorders
48. Clinical Evaluation Of Laporoscopic Surgery For Children With Persistent Cloaca And Whole-exome Sequencing Screen In Human Persistent Cloaca
49. Paradoxical Reactions Of β-Catenin To TNF-α And Fas-induced Acute Liver Failure
50. Study Of Biomarkers For Molecular Classification In Hepatocellular Carcinoma And Prostate Cancer
51. Explore The Mechanism Of Prostate Cancer Recurrence By RNA Sequencing And Whole Exome Sequencing
52. Spectrum Of Congenital Heart Disease In Yangbi County Of Yunnan Province And Identification Of Candidate Atrial Septal Defect Predisposing Gene Variants In Sporadic Atrial Septal Defect Using Whole Exome Sequencing
53. A Genome-wide Association Study For Coding Variants Of Psoriasis
54. Whole-exome Sequencing Identifiy Novel Mutations In Caustive Gene EYS For RP And Function Study Of Causitive Gene For PCG
55. Identification Of Novel Pathogenic Genes And Study Of Their Mechanisms In Monogenic Disorders
56. Whole Exome Sequencing To Identify Novel Gene Mutations Associated With Postoperative Relapse Of Node Negative Thoracic Esophageal Squamous Cell Carcinoma
57. Mutation Spectrum Of Retnet Genes In Probands With Retinitis Pigmentosa And Associated Diseases
58. The Exploring Study On Predisposing Genes Of Intracranial Aneurysm Patients
59. A Novel Missense SNRNP200Mutation Associated With Autosomal Dominant Retinitis Pigmentosa In A Chinese Family
60. Identification Of The Causative Gene Of A DSAP Edigree Using Exome Sequencing
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