No abstract available
MeSH terms
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Adolescent
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Female
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Humans
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Mutation*
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Noonan Syndrome / complications*
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Noonan Syndrome / genetics*
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Phenotype
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SOS1 Protein / genetics*
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Synovitis, Pigmented Villonodular / complications*
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Synovitis, Pigmented Villonodular / genetics*
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Synovitis, Pigmented Villonodular / pathology