No abstract available
MeSH terms
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Abnormalities, Multiple / genetics*
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Child
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Chromosome Aberrations*
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Chromosome Inversion / genetics*
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Chromosomes, Human, Pair 10 / genetics*
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Female
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Gene Duplication*
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Humans
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Infant
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Infant, Newborn
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Phenotype
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Pregnancy
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Syndrome
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Trisomy / genetics*