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Q48104462-03535FA3-8173-46F3-9681-9E6FBB1ADD7E
Q48104462-03535FA3-8173-46F3-9681-9E6FBB1ADD7E
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http://www.wikidata.org/entity/statement/Q48104462-03535FA3-8173-46F3-9681-9E6FBB1ADD7E
Mutations and karyotype in myelodysplastic syndromes: TP53 clusters with monosomal karyotype, RUNX1 with trisomy 21, and SF3B1 with inv(3)(q21q26.2) and del(11q).
P2860
Q48104462-03535FA3-8173-46F3-9681-9E6FBB1ADD7E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48104462-03535FA3-8173-46F3-9681-9E6FBB1ADD7E
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wasDerivedFrom
5b6fd7312243c392b11d2ffa0ecb46796319e6f8
P2860
High frequency of RUNX1 mutation in myelodysplastic syndrome patients with whole-arm translocation of der(1;7)(q10;p10).