copy number variants - Globe Thesis

Keyword [copy number variants] Result: 1 - 20 \| Page: 1 of 2
1.	Effects Of Environmental Endocrine Disruptors On The Characteristics Of Neuroblastoma Cells And Whole Genomic Copy Number Variant Profiling Of Neuroblastoma
2.	Retrospective Clinical Study And Genome-Wide Copy Number Variants Analysis On Congenital Pulmonary Atresia With Ventricular Septal Defect
3.	Detection Of Copy Number Variants In The α-globin Gene Cluster And Molecular Diagnosis Of Common Deletions Withα-thalassemia In Chinese
4.	Integrative Analysis Of "OMICS" Data Of Hepatocellular Carcinoma And De Novo Germline Copy Number Variants In Hepatocellular Carcinoma
5.	The Application Of Array-based Comparative Genomic Hybridization In Birth Defects
6.	Chromosomal Microarray Analysis In The Prenatal Genetic Diagnosis Of Fetal Multicystic Dysplastic Kidney
7.	SNP Array-based Genome-wide Assessment Of Rare Copy Number Variants In Colorectal Cancer And Exploration Of Clinical Significance Of Relevant Genes
8.	Impact Of Syndrome And CNVs On The Outcome Of Surgery Of Conotruncal Heart Defects
9.	Identification Of Copy Number Variants In Couples With Unexplained Recurrent Miscarriage And Predictive Value Of HCG In Pregnancy Outcome
10.	Application Of Chromosome Microarray Investigated Fetuses With Common Urinary Abnormalities
11.	Copy Number Variants And Genetic Polymorphisms In TBX21, GATA3, Rorc, Foxp3 And Susceptibility To Behcet’s Disease And Vogt-Koyanagi-Harada Syndrome
12.	Analysis Of Chromosomal Aberrations In Fetuses With Congenital Heart Malformations
13.	Genetic Variations Of IL17F And IL23A Show Associations With Behcet’s Disease And Vogt-koyanagi-harada Syndrome
14.	Copy Number Variants Analysis And The Related Gene In Chinese Han Women With Premature Ovarian Failure
15.	Copy Number Variants Analysis And Clinical Effectiveness In Patients With Lipoma Tethered Cord Syndrome
16.	MicroRNA Copy Number Variants Confer The Susceptibility To Acute Anterior Uveitis With Or Without Ankylosing Spondylitis
17.	The Association Between De Novo Sequence/copy Number Variants And Tourette Disorder
18.	Application Of Next-generation Sequencing On Study Genomic Structural Variants
19.	A New Method For Evaluate The Fetal Conus Medullaris Position By Ultrasound And Explore Copy Number Variants In Tethered Cord Fetuses
20.	A Pericentric Inversion Of Chromosome X Disrupting F8 And Resulting In Severe Haemophilia
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