Barely Significant
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Multiplex Approach in Classification, Diagnosis, and Prognostication in Acute Myeloid Leukemia: An Experience from Tertiary Cancer Center in South India.

Indian J Med Paediatr Oncol · 2017 · PMC5686964 · PMID 29200671

1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantP < 0.0001actually significant
Frequency of FLT3/ITD in patients with normal karyotype (NK) was 21%, while none of the patients with abnormal karyotype showed this mutation, difference being highly significant ( P < 0.0001).

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