No abstract available
MeSH terms
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Chromosome Deletion*
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Chromosomes, Human, Pair 22*
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DiGeorge Syndrome / genetics
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Female
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Genetic Diseases, Inborn / genetics*
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Genetic Markers
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Heart Defects, Congenital / genetics
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Humans
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In Situ Hybridization, Fluorescence
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Male
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Syndrome
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Velopharyngeal Insufficiency / genetics