No abstract available
MeSH terms
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Acute Disease
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Child
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Chromosome Deletion*
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Chromosomes, Human, Pair 20*
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Chromosomes, Human, Pair 7*
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Exocrine Pancreatic Insufficiency / diagnosis
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Exocrine Pancreatic Insufficiency / genetics*
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Humans
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Karyotyping
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Leukemia, Myeloid / genetics
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Male
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Monosomy
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Myelodysplastic Syndromes / genetics
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Syndrome