No abstract available
MeSH terms
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Abnormalities, Multiple / genetics*
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Child, Preschool
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Chromosome Deletion*
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Chromosomes, Human, Pair 10 / genetics*
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Craniofacial Abnormalities / genetics
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Developmental Disabilities / genetics*
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Humans
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In Situ Hybridization, Fluorescence
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Male
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Monosomy
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Oligonucleotide Array Sequence Analysis