No abstract available
MeSH terms
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Acute Disease
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Child, Preschool
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Chromosomes, Human, Pair 21 / genetics*
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Disease Susceptibility
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Female
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Genes, Dominant
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Genotype
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Hemorrhagic Disorders / etiology
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Humans
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Leukemia, Myeloid / epidemiology
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Leukemia, Myeloid / etiology*
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Lod Score
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Male
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Pedigree
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Phenotype
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Risk
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Thrombocytopenia / complications
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Thrombocytopenia / genetics*