Source: European journal of medical genetics. Unidade: FM
Subjects: NEOPLASIAS OVARIANAS, MUTAÇÃO GENÉTICA, ANEMIA
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FREIRE, Bruna L. et al. Homozygous loss of function BRCA1 variant causing a Fanconi-anemia-like phenotype, a clinical report and review of previous patients. European journal of medical genetics, v. 61, n. 3, p. 130-133, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2017.11.003. Acesso em: 30 set. 2024.APA
Freire, B. L., Homma, T. K., Funari, M. F. A., Lerario, A. M., Leal, A. M., Velloso, E. D. R. P., et al. (2018). Homozygous loss of function BRCA1 variant causing a Fanconi-anemia-like phenotype, a clinical report and review of previous patients. European journal of medical genetics, 61( 3), 130-133. doi:10.1016/j.ejmg.2017.11.003NLM
Freire BL, Homma TK, Funari MFA, Lerario AM, Leal AM, Velloso EDRP, Malaquias AC, Jorge AA de L. Homozygous loss of function BRCA1 variant causing a Fanconi-anemia-like phenotype, a clinical report and review of previous patients [Internet]. European journal of medical genetics. 2018 ; 61( 3): 130-133.[citado 2024 set. 30 ] Available from: https://doi.org/10.1016/j.ejmg.2017.11.003Vancouver
Freire BL, Homma TK, Funari MFA, Lerario AM, Leal AM, Velloso EDRP, Malaquias AC, Jorge AA de L. Homozygous loss of function BRCA1 variant causing a Fanconi-anemia-like phenotype, a clinical report and review of previous patients [Internet]. European journal of medical genetics. 2018 ; 61( 3): 130-133.[citado 2024 set. 30 ] Available from: https://doi.org/10.1016/j.ejmg.2017.11.003