No abstract available
MeSH terms
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Adult
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Camurati-Engelmann Syndrome / genetics*
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Chromosome Deletion*
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Chromosomes, Human, Pair 9 / genetics*
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Femoral Neoplasms / genetics*
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Histiocytoma, Benign Fibrous / genetics*
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Humans
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Loss of Heterozygosity / genetics*
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Male
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Pedigree