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Incidence and clinical significance of FLT3 and nucleophosmin mutation in childhood acute myeloid leukemia in Chile.
Hematol Transfus Cell Ther. 2023 Jan-Mar;45(1):77-82. doi: 10.1016/j.htct.2021.06.003. Epub 2021 Jul 30.
Hematol Transfus Cell Ther. 2023.
PMID: 34690101
Free PMC article.
[Congenital anomalies of poor prognosis. Genetics Consensus Committee].
Pardo Vargas RA, Aracena M, Aravena T, Cares C, Cortés F, Faundes V, Mellado C, Passalacqua C, Sanz P, Castillo Taucher S.
Pardo Vargas RA, et al. Among authors: cares c.
Rev Chil Pediatr. 2016 Sep-Oct;87(5):422-431. doi: 10.1016/j.rchipe.2016.04.005. Epub 2016 May 24.
Rev Chil Pediatr. 2016.
PMID: 27234469
Free article.
Spanish.
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Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in Chile.
Poli MC, Rebolledo-Jaramillo B, Lagos C, Orellana J, Moreno G, Martín LM, Encina G, Böhme D, Faundes V, Zavala MJ, Hasbún T, Fischer S, Brito F, Araya D, Lira M, de la Cruz J, Astudillo C, Lay-Son G, Cares C, Aracena M, Martin ES, Coban-Akdemir Z, Posey JE, Lupski JR, Repetto GM.
Poli MC, et al. Among authors: cares c.
Eur J Hum Genet. 2024 Jan 4. doi: 10.1038/s41431-023-01523-5. Online ahead of print.
Eur J Hum Genet. 2024.
PMID: 38177409
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