Role of copy number variants in structural birth defects

Keyphrases

• Copy number Variation 100%
• Structural Birth Defects 100%
• Birth Defects 18%
• Array Comparative Genomic Hybridization (aCGH) 18%
• Renal System 18%
• Respiratory System 18%
• Cardiac System 18%
• Craniofacial System 18%
• Specific Locus 9%
• Patient Care 9%
• Gene Locus 9%
• Pathologic 9%
• Evidence Support 9%
• Genetic Testing 9%
• Search Terms 9%
• Aberrations 9%
• Genetic Counseling 9%
• Human Genome 9%
• Disease Phenotype 9%
• Congenital Heart Disease 9%
• SNP Array 9%
• Structural Defects 9%
• PubMed Database 9%
• Structural Anomalies 9%
• Craniofacial Defects 9%
• Renal Defects 9%
• Neurocognitive Deficits 9%
• Languages Other than English 9%
• Variant Detection 9%
• Pathogenic Copy number Variant (pCNV) 9%

Biochemistry, Genetics and Molecular Biology

• Array Comparative Genomic Hybridization 100%
• Single-Nucleotide Polymorphism 50%
• Human Genome 50%
• Copy-Number Variation 50%
• Medline 50%
• Genetic Screening 50%
• Genetic Counseling 50%