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- W2022110372 abstract "Abstract Ollier disease is a rare disorder characterized by the presence of multiple enchondromas and a propensity to develop malignancies. We report the case of a 7‐year‐old Caucasian male with Ollier disease who developed acute myelogenous leukemia (AML). This report describes a patient with Ollier disease and AML and may offer a clue into the genetic pathogenesis of these disorders. Pediatr Blood Cancer 2008;50:645–646. © 2006 Wiley‐Liss, Inc." @default.
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- W2022110372 date "2008-01-09" @default.
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- W2022110372 title "Acute myelogenous leukemia associated with Ollier disease" @default.
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- W2022110372 doi "https://doi.org/10.1002/pbc.21050" @default.
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