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Q33702150-A1F3632F-0ECC-41A4-A0F5-CAB802617EA3
Q33702150-A1F3632F-0ECC-41A4-A0F5-CAB802617EA3
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Statement
http://www.wikidata.org/entity/statement/Q33702150-A1F3632F-0ECC-41A4-A0F5-CAB802617EA3
Copy-neutral loss of heterozygosity is prevalent and a late event in the pathogenesis of FLT3/ITD AML
P2860
Q33702150-A1F3632F-0ECC-41A4-A0F5-CAB802617EA3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33702150-A1F3632F-0ECC-41A4-A0F5-CAB802617EA3
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wasDerivedFrom
548b7bf547f39a5a50ed1ee5392fee6dfbfe257d
P2860
SNP array analysis of acute promyelocytic leukemia may be of prognostic relevance and identifies a potential high risk group with recurrent deletions on chromosomal subband 1q31.3.