No abstract available
MeSH terms
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Abnormalities, Multiple / genetics
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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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DiGeorge Syndrome / pathology*
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Facial Bones / abnormalities
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Heart Defects, Congenital / genetics
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Humans
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Kidney / abnormalities*
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Phenotype