No abstract available
MeSH terms
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Child
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Chromosomes, Human, Pair 4 / genetics*
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Fragile X Mental Retardation Protein / genetics
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Humans
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Intellectual Disability / genetics*
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Language Development Disorders / genetics*
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Male
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Uniparental Disomy / genetics*
Substances
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FMR1 protein, human
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Fragile X Mental Retardation Protein