No abstract available
MeSH terms
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Beckwith-Wiedemann Syndrome / genetics
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Extrachromosomal Inheritance / genetics
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Fragile X Syndrome / genetics
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Genetic Diseases, Inborn / genetics*
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Genetics, Medical
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Genomic Imprinting
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Genotype
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Humans
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Inheritance Patterns / genetics*
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Multifactorial Inheritance / genetics
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Mutation / genetics*
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Phenotype
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Trinucleotide Repeat Expansion
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Uniparental Disomy / genetics