No abstract available
MeSH terms
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Child
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Chromosome Aberrations / genetics*
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Chromosome Disorders
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Chromosomes, Human, Pair 1
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DNA Mutational Analysis
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Genes, Dominant / genetics*
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Humans
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Lamins
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Muscular Dystrophy, Emery-Dreifuss / genetics*
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Nuclear Envelope / genetics*
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Nuclear Proteins / genetics*
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Phenotype