No abstract available
MeSH terms
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Chromosome Mapping
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Deoxyribonucleases, Type II Site-Specific
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Fragile X Syndrome / genetics*
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Gene Frequency
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Genetic Markers*
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Humans
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Polymorphism, Restriction Fragment Length*
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Sex Chromosome Aberrations / genetics*
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X Chromosome*
Substances
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Genetic Markers
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endodeoxyribonuclease XmnI
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Deoxyribonucleases, Type II Site-Specific