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

✍ Scribed by Enshaei, A; Schwab, C J; Konn, Z J; Mitchell, C D; Kinsey, S E; Wade, R; Vora, A; Harrison, C J; Moorman, A V


Book ID
120807606
Publisher
Nature Publishing Group
Year
2013
Tongue
English
Weight
186 KB
Volume
27
Category
Article
ISSN
0887-6924

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