Abstract
Fluorescence in situ hybridization with a telomeric probe was used to monitor telomeric renewal following breakage induced by the rare fragile sites FRA10A, FRA12A and FRA16B. Interstitial telomere-like sequences were detected only at the break sites of FRA10A.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Chromosome Aberrations / genetics*
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Chromosome Deletion
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Chromosome Disorders
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Chromosome Fragile Sites
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Chromosome Fragility*
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Chromosomes, Human, Pair 10
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Chromosomes, Human, Pair 12
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Chromosomes, Human, Pair 16
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DNA Probes
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Female
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Humans
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In Situ Hybridization, Fluorescence
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Infant, Newborn
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Male
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Telomere / genetics*