No abstract available
MeSH terms
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Abnormalities, Multiple / genetics
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Chromosome Aberrations / genetics*
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Chromosome Disorders
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Chromosomes, Human, 16-18*
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Chromosomes, Human, 6-12 and X
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Dermatoglyphics
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Female
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Humans
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Infant
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Infant, Newborn
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Karyotyping
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Trisomy*