No abstract available
MeSH terms
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Chromosome Fragility
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Chromosome Mapping
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Chromosomes, Human, Pair 14 / ultrastructure
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Female
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Fragile X Messenger Ribonucleoprotein 1
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Fragile X Syndrome / classification
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Fragile X Syndrome / genetics
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Gene Expression Regulation
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Genetic Diseases, Inborn / genetics*
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Humans
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Machado-Joseph Disease / genetics
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Male
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Methylation
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Minisatellite Repeats*
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Mutation*
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Nerve Tissue Proteins / genetics
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RNA-Binding Proteins*
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X Chromosome / ultrastructure
Substances
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Fragile X Messenger Ribonucleoprotein 1
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Nerve Tissue Proteins
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RNA-Binding Proteins
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FMR1 protein, human