whole-exome sequencing - Globe Thesis

Keyword [whole-exome sequencing] Result: 21 - 40 \| Page: 2 of 10
21.	Effects Of Cell Division Cycle Associated 2 And Its Mechanism Research In Pancreatic Ductal Adenocarcinoma
22.	Clinical Evaluation Of Laporoscopic Surgery For Children With Persistent Cloaca And Whole-exome Sequencing Screen In Human Persistent Cloaca
23.	Study Of Biomarkers For Molecular Classification In Hepatocellular Carcinoma And Prostate Cancer
24.	Explore The Mechanism Of Prostate Cancer Recurrence By RNA Sequencing And Whole Exome Sequencing
25.	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
26.	Whole-exome Sequencing Identifiy Novel Mutations In Caustive Gene EYS For RP And Function Study Of Causitive Gene For PCG
27.	Identification Of Novel Pathogenic Genes And Study Of Their Mechanisms In Monogenic Disorders
28.	Whole Exome Sequencing To Identify Novel Gene Mutations Associated With Postoperative Relapse Of Node Negative Thoracic Esophageal Squamous Cell Carcinoma
29.	Mutation Spectrum Of Retnet Genes In Probands With Retinitis Pigmentosa And Associated Diseases
30.	The Exploring Study On Predisposing Genes Of Intracranial Aneurysm Patients
31.	Exome Sequencing Revealed Novel Germline Mutations In Chinese Peutz-Jeghers Syndrome Patients
32.	Exome Sequencing Identifies Novel Compound Heterozygous Mutations In SPG11That Cause Autosomal Recessive Hereditary Spastic Paraplegia
33.	A Study On Whole Exome Sequence Data Analysis And Its Application In Hepatocellular Carcinoma
34.	Diagnosis Of A Recessive Progressive Myoclonic Epilepsy Pedigree By Using Whole Exome Sequencing
35.	A Preliminary Study Of Identifying The Causative Gene Of A Schizophrenia Pedigree
36.	Searching For The Pathogenic Variant Of A Olmsted Syndrome-like Pedigree By Whole Exome Sequencing
37.	A Pilot Study Of Human Whole-exome Sequencing On Gene Chip For Oral Cancer SNPS
38.	Whole Exome Sequencing Identifying Genetic Etiology Of Congenital Scoliosis In Chinese Han Population
39.	Whole Exome Sequencing Identifying Causative Gene In A Intracranial Aneurysm Pedigree
40.	1, Part I: Gene Pathogenic Female Reproductive Tract Abnormalities In Patients 2, Part II: Clinical Phenotype, Family History Research 98 Cases Of Chinese MRKH Syndrome And Psychological Functions
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