Long-term follow-up of ETV6-RUNX1 ALL reveals that NCI risk, rather than secondary genetic abnormalities, is the key risk factor

A. Enshaei, C. J. Schwab, Z. J. Konn, C. D. Mitchell, S. E. Kinsey, R. Wade, A. Vora, C. J. Harrison, A. V. Moorman

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