No abstract available
MeSH terms
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Base Pairing / genetics*
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Chromosome Disorders / complications
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Chromosome Disorders / genetics
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Chromosomes, Human, Pair 13 / genetics
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Chromosomes, Human, Pair 4 / 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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Microarray Analysis*
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Polydactyly / complications*
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Polydactyly / genetics*
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Translocation, Genetic*
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Trisomy / genetics
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Trisomy 13 Syndrome
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Wolf-Hirschhorn Syndrome / complications
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Wolf-Hirschhorn Syndrome / genetics