No abstract available
MeSH terms
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Chromosomes, Human, Pair 17 / genetics*
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Chromosomes, Human, Pair 4 / genetics*
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Deaf-Blind Disorders / classification*
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Deaf-Blind Disorders / genetics*
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Epilepsy / classification*
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Epilepsy / genetics*
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Growth Disorders / classification*
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Growth Disorders / genetics*
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Humans
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In Situ Hybridization, Fluorescence
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Male
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Mental Retardation, X-Linked / classification*
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Mental Retardation, X-Linked / genetics*
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Microarray Analysis / methods
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Translocation, Genetic / genetics*
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Wolf-Hirschhorn Syndrome / genetics*