No abstract available
MeSH terms
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Aorta, Thoracic / abnormalities
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Child
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Chromosome Deletion*
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Chromosomes, Human, Pair 22 / genetics*
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DiGeorge Syndrome / genetics
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Face / abnormalities
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Genetic Counseling*
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Heart Defects, Congenital / genetics
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Heart Septal Defects, Ventricular / genetics
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Humans
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In Situ Hybridization, Fluorescence
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Outcome Assessment, Health Care
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Phenotype
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Risk Factors
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Syndrome
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Tetralogy of Fallot / genetics
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Truncus Arteriosus, Persistent / genetics