No abstract available
MeSH terms
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Abnormalities, Multiple / genetics*
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Female
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Fibrillin-1
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Fibrillins
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Gene Frequency
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Heart Defects, Congenital / genetics
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Heterozygote
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Humans
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Japan
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Male
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Microfilament Proteins / genetics*
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Mutation*
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Restriction Mapping
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Syndrome
Substances
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FBN1 protein, human
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Fibrillin-1
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Fibrillins
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Microfilament Proteins