No abstract available
MeSH terms
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Abnormalities, Multiple / genetics
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Child
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Chromosomes, Human, Pair 7 / genetics*
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Craniofacial Abnormalities / genetics
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Female
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Humans
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In Situ Hybridization, Fluorescence
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Language Development Disorders / genetics
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Mosaicism*
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Phenotype
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Ring Chromosomes*
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Syndrome
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Williams Syndrome / genetics