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Keyword [CNVS]
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1. MRI Study On Brain Neuronetwork Connections In Early Onset Schizophrenia And DNA Copy Number Variations In Major Psychosis
2. Candidate Genes Validation And Genome-wide Association Study In Pathological Myopia Patients And Nuclear Pedigrees
3. Identification Of X-linked Congenital Generalized Hair Histiocytosis Pathogenic Mutation
4. Surgical Treatment And CNVs Analysis Of Pulmonary Atresia
5. Association Study Of NRXN1Gene And Identification Of Two CNVs Associated With Autism In Chinese Han Population
6. Identification Of The Causative CNVs In Syndromic Congenital Heart Defects By High Resolution Array-SNP
7. Licorice Hmgr, Sqs, Beta-as Synthase Gene Cnvs Origin, Morphology Study
8. Preliminary Study Of Molecular Diagnosis In Some Rare Genetics Disorders Of Neonatal
9. Application Research Of Prenatal Diagnosis For Genome-wide Copy Number Variations(CNVs) In The High-throughput Sequencing Abnormal Signals Analysis
10. SNP Array-based Genome-wide Assessment Of Rare Copy Number Variants In Colorectal Cancer And Exploration Of Clinical Significance Of Relevant Genes
11. Licorice Hmgr, Sqs1 And Beta Contents As Gene Cnvs And Glycyrrhizic Acid, Licorice Correlation Studies
12. Licorice Hmgr, Sqs1 And Beta As Gene Cnvs System Construction
13. Impact Of Syndrome And CNVs On The Outcome Of Surgery Of Conotruncal Heart Defects
14. Gene Mutation And CNVs Analysis For Congenital Heart Defects With Limb Anomalies
15. Studies On Copy Number Variations And Screening Related Genes In Xuanwei Lung Cancer
16. CNVs Analysis For Congenital Heart Disease
17. Association Of BACG-1, BACH-2, NRF-1 Copy Number Variation With BD And VKH Syndrome
18. Copy Number Variants Analysis And The Related Gene In Chinese Han Women With Premature Ovarian Failure
19. Prognosis Studies And Verification Studies Of The Genome-wide Copy Number Variations With Landau-Kleffner Syndrome
20. Copy Number Variation Detection On Multi-core Platform And Parallel Algorithm
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