Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS

Keyphrases

• Psychiatric Disorders 100%
• Gene-rich Regions 100%
• 22q11.2 Deletion Syndrome 100%
• Common Haplotype 100%
• COMT Gene 100%
• Attention Deficit Hyperactivity Disorder 50%
• Obsessive-compulsive Disorder 50%
• SNP 20%
• High-risk HPV 20%
• Risk Factors 10%
• High Prevalence 10%
• Functional Variation 10%
• Common Risks 10%
• Genetic Predisposition 10%
• IQ Score 10%
• Linkage Disequilibrium 10%
• Parent-of-origin 10%
• Deletion Syndrome 10%
• Gene Variation 10%
• Homozygous Deletion 10%
• Physical Abnormalities 10%
• Rs4680 10%
• Low Activity 10%

Biochemistry, Genetics and Molecular Biology

• Haplotype 100%
• Single Nucleotide Polymorphism 33%
• Population 33%
• Genetic Predisposition 16%
• Rs4680 16%
• Prevalence 16%
• Allele 16%
• Gene Linkage Disequilibrium 16%