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Acute Erythroid Leukemia
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Revision as of 15:21, 10 May 2018
209 bytes added
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15:21, 10 May 2018
→Gene Mutations (SNV/INDEL)
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==Gene Mutations (SNV/INDEL)==
==Gene Mutations (SNV/INDEL)==
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Not Applicable
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Intraclonal heterogeneity and founder mutations of TP53 were reported in 92% (11 out of 12 cases) while co-occurrence of TP53 mutation and deletion due to chromosome 17p abnormalities was detected in 73% of PEL cases [13].
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Ashwiniy
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