Bousquets Muñoz, PabloMolina, ÒscarVarela, IgnacioÁlvarez-Eguiluz, ÁngelFernández-Mateos, JavierGómez, AnaSánchez, Elena G.Balbín, MilagrosRuano, DavidRamírez-Orellana, ManuelPuente, Xose S.Menéndez, PabloVelasco-Hernandez, Talia2025-02-052025-02-052024-05-170887-6924https://hdl.handle.net/2445/218527This work demonstrated the prenatal origin of the translocation t(7;12) giving rise to the ETV6-NOM1 fusion protein, in a 5-month-old patient with acute myeloblastic leukemia using an umbilical cord blood (CB) sample from the patient stored at birth. Our findings revealed the presence of a specific t(7;12)/ETV6-NOM1 fusion in both CD34+ hematopoietic stem/progenitor cells and in the CD34-CD33+ myeloid cellular compartment isolated from the patient’s umbilical CB.5 p.application/pdfengcc by (c) Bousquets-Muñoz, P. et al., 2024https://creativecommons.org/licenses/by/4.0/Leucèmia mieloideCromosomes humansInfantsMyeloid leukemiaHuman chromosomesChildrenBacktracking NOM1::ETV6 fusion to neonatal pathogenesis of t(7;12) (q36;p13) infant AML.info:eu-repo/semantics/article7527202025-02-05info:eu-repo/semantics/openAccess38806630