Genotypic and phenotypic variability of 22q11.2 microduplications: An institutional experience

Keyphrases

• Phenotypic Variation 100%
• Institutional Experience 100%
• Genotypic Variability 100%
• 22q11.2 Deletion Syndrome 100%
• 22q11.2 Microduplication 100%
• Neonate 50%
• Clinical Phenotype 50%
• Clinical Features 50%
• Central Nervous System 50%
• Duplication 50%
• Pediatric Patients 50%
• Healthy Adults 50%
• Developmental Delay 50%
• Congenital Abnormalities 50%
• Genotype-phenotype 50%
• Cardiovascular Defects 50%
• Chromosomal Microarray 50%
• Facial Abnormalities 50%
• Duplicated Region 50%
• 22q11.2 Duplication 50%
• System Delay 50%

Biochemistry, Genetics and Molecular Biology

• Normal Human 100%
• Microarrays 100%