Genotype-phenotype correlation in 22q11.2 deletion syndrome

Keyphrases

• 22q11.2 Deletion Syndrome 100%
• Genotype-phenotype Correlation 100%
• Molecular Methods 40%
• High-resolution 20%
• Redundancy 20%
• Molecular Characterization 20%
• Physical Symptoms 20%
• Cognitive Evaluation 20%
• Clinical Manifestations 20%
• Clinical Data 20%
• Clinical Evaluation 20%
• Accurate Diagnosis 20%
• Molecular Analysis 20%
• Genotype-phenotype 20%
• Biological Mechanisms 20%
• Clinical Assessment 20%
• Clinical Standards 20%
• Genotype-phenotype Association 20%
• Psychiatric Assessment 20%
• Neuropsychiatric Manifestations 20%
• Hemizygous 20%
• Hypocalcemia 20%
• Microdeletion 20%
• Physical Manifestations 20%
• Chromosome 22q11.2 20%
• Physical Phenotype 20%
• Cardiovascular Anomalies 20%
• Neuropsychiatric Phenotype 20%
• Cognitive Trajectory 20%
• Multicenter Collaboration 20%

Biochemistry, Genetics and Molecular Biology

• Genotyping 100%
• Genotype Phenotype Correlation 100%
• Multiplex Ligation-Dependent Probe Amplification 100%
• Clinical Trial 50%
• Hypocalcaemia 50%