No abstract available
MeSH terms
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Abnormalities, Multiple / genetics*
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Brain / pathology
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Chromosomes, Human, Pair 18*
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Chromosomes, Human, Pair 8*
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Craniofacial Abnormalities / genetics*
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Cytogenetics
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Facies
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Female
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Fetal Growth Retardation
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Humans
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In Situ Hybridization, Fluorescence
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Infant
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Karyotyping
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Male
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Pregnancy
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Syndrome
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Translocation, Genetic*