Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia (2018)
- Authors:
- USP affiliated authors: ROCHA, VANDERSON GERALDO - FM ; VELLOSO, ELVIRA DEOLINDA RODRIGUES PEREIRA - FM
- Unidade: FM
- DOI: 10.1016/j.cancergen.2018.01.002
- Subjects: TROMBOCITOPENIA; LEUCEMIA; DOENÇAS GENÉTICAS; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Cancer genetics
- ISSN: 2210-7762
- Volume/Número/Paginação/Ano: v. 222, p. 32-37, 2018
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
SILVA, Marcela Cavalcante de Andrade e ROCHA, Vanderson e VELLOSO, Elvira Deolinda Rodrigues Pereira. Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia. Cancer genetics, v. 222, p. 32-37, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.cancergen.2018.01.002. Acesso em: 05 out. 2024. -
APA
Silva, M. C. de A., Rocha, V., & Velloso, E. D. R. P. (2018). Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia. Cancer genetics, 222, 32-37. doi:10.1016/j.cancergen.2018.01.002 -
NLM
Silva MC de A, Rocha V, Velloso EDRP. Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia [Internet]. Cancer genetics. 2018 ; 222 32-37.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.cancergen.2018.01.002 -
Vancouver
Silva MC de A, Rocha V, Velloso EDRP. Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia [Internet]. Cancer genetics. 2018 ; 222 32-37.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.cancergen.2018.01.002 - Salvage treatment for refractory or relapsed acute myeloid leukemia: a 10-year single-center experience
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Informações sobre o DOI: 10.1016/j.cancergen.2018.01.002 (Fonte: oaDOI API)
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