No abstract available
MeSH terms
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Abnormalities, Multiple / genetics*
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Brain / abnormalities*
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Chromosomes, Human, 13-15*
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Chromosomes, Human, 6-12 and X
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Heart Defects, Congenital / genetics*
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Humans
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Infant, Newborn
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Karyotyping
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Male
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Skull / abnormalities*
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Syndrome
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Translocation, Genetic
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Trisomy*