Prevalence and parental origin in tetralogy of fallot associated with chromosome 22q11 microdeletion

Medicine and Dentistry

• Prevalence 100%
• Tetralogy of Fallot 100%
• Patient with Tetralogy of Fallot 66%
• Clinical Trial 33%
• Heart Disease 33%
• Real-Time Polymerase Chain Reaction 33%
• Autosomal Dominant Inheritance 33%
• Microsatellite Marker 33%
• Pulmonary Atresia 33%
• Pulmonary Valve Stenosis 33%
• Hemizygosity 33%

Biochemistry, Genetics and Molecular Biology

• Prevalence 100%
• Genotyping 50%
• Clinical Trial 50%
• Real-Time Polymerase Chain Reaction 50%
• Microsatellite Marker 50%
• Autosomal Dominant Inheritance 50%
• Hemizygosity 50%