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Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11

ChromatinMendelian DisorderGenetic DisorderMedicineNf1 LocusGeneticsPathologyDisease Gene IdentificationMolecular DiagnosticsMutant RasMyeloid Neoplasia