Copy Number Variation - Globe Thesis

Keyword [Copy Number Variation] Result: 181 - 200 \| Page: 10 of 10
181.	The Associations Between Copy Number Variation In Triple Negative Breast Cancer Gene And Clinicopathological Characteristic On The Prognosis Of Patients
182.	Prognostic Value Of Plasma Free DNA In Breast Cancer
183.	Study Of Using UPIP-qPCR Technology To Develop SNP Detection Kit Of Deafness Gene And New CNV Detection Method
184.	Integrating Genomic Features To Predict The Therapeutic Efficacy And Prognosis In Patients With Platinum-resistant Ovarian Cancer And Metastatic Neuroendocrine Neoplasms
185.	Research On Cancer Copy Number Variation Detection Methods For Next-Generation Sequencing Data
186.	To Explore The Heterogeneity And Clinical Significance Of Clear Cell Renal Cell Carcinoma At The Single Cell Resolution
187.	The Pathogenic Role And Mechanism Of CEL-HYB Variants In Chronic Pancreatitis
188.	Clinical Application Of Noninvasive Prenatal Testing For Screening Fetal Chromosome Aneuploidy And Prenatal Diagnosis In Twin Pregnancies
189.	Integrated Single-cell Transcriptomics Study Of Refractory/relapsed Childhood Acute B Lymphoblastic Leckemia
190.	Study On The Association And Mechanism Between The Copy Number Variation Of PLA2G4A And Susceptibility To Schizophrenia
191.	The Role Of Structural Cells In Shaping The Microenvironment Of Bladder Cancer
192.	The Landscape Of Somatic Mutations And The Functions Of Major Mutant Genes In Acral Melanoma
193.	Clinical Application Of Non-invasive Prenatal Testing Technology For Fetal Chromosome Copy Number Variation Detection
194.	Identification Of Pathogenic Mutations In Deficiency Of Adenosine Deaminase 2 And Autoimmune Disease,Multisystem,Infantile-Onset,1
195.	Analysis Of Genetical Cause Of Three Hereditary Hemolytic Anemia Families
196.	Reduction Of False Positive Rate Based On Quantification Of Fetal Cell Free DNA Fraction And Expand Application Scope In Noninvasive Prenatal Test
197.	Population-based Multiomics Systematic Analysis Of The Role Of Endogenous IFN-λ In Cancer Progression And Immune Evasion
198.	Chromosome Abnormality Analysis Of Missed Abortion Tissue In Western Yunnan Plateau
199.	Clinical Study Of Copy Number Variation In The Etiological Diagnosis Of Fetal Congenital Heart Disease
200.	ANAPC11 Drives The Malignant Phenotype Of Glioblastoma Cells
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