Abstract
A case of an infant with ring chromosome 5 is presented. The phenotype of this patient and other reported cases is analyzed with respect to the deletion of the long arm of chromosome 5.
MeSH terms
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Abnormalities, Multiple / genetics*
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Chromosome Aberrations*
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Chromosome Deletion
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Chromosomes, Human, Pair 5*
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Humans
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Infant
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Karyotyping
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Male
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Phenotype
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Ring Chromosomes*