No abstract available
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Cell Line
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Centromere
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Chromosome Mapping
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Chromosomes, Human, Pair 22*
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Congenital Abnormalities / genetics*
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Genetic Markers
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Humans
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In Situ Hybridization, Fluorescence
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Sequence Deletion*
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Syndrome