Does DKC1 mutation suffice to define the phenotype severity of hoyeraal-hreidarsson syndrome? (2013)
Source: Open Journal of Blood Diseases. Unidade: FMRP
Subjects: MEDULA ÓSSEA, MUTAÇÃO GENÉTICA
ABNT
VALERA, Elvis Terci et al. Does DKC1 mutation suffice to define the phenotype severity of hoyeraal-hreidarsson syndrome?. Open Journal of Blood Diseases, v. 3, n. 1, p. 57-61, 2013Tradução . . Disponível em: https://doi.org/10.4236/ojbd.2013.31012. Acesso em: 11 maio 2024.APA
Valera, E. T., Brassesco, M. S., Ferraz, S. T., Roxo Junior, P., Santana, B. L., Vulliamy, T., et al. (2013). Does DKC1 mutation suffice to define the phenotype severity of hoyeraal-hreidarsson syndrome? Open Journal of Blood Diseases, 3( 1), 57-61. doi:10.4236/ojbd.2013.31012NLM
Valera ET, Brassesco MS, Ferraz ST, Roxo Junior P, Santana BL, Vulliamy T, Calado RT, Scrideli CA, Tone LG. Does DKC1 mutation suffice to define the phenotype severity of hoyeraal-hreidarsson syndrome? [Internet]. Open Journal of Blood Diseases. 2013 ; 3( 1): 57-61.[citado 2024 maio 11 ] Available from: https://doi.org/10.4236/ojbd.2013.31012Vancouver
Valera ET, Brassesco MS, Ferraz ST, Roxo Junior P, Santana BL, Vulliamy T, Calado RT, Scrideli CA, Tone LG. Does DKC1 mutation suffice to define the phenotype severity of hoyeraal-hreidarsson syndrome? [Internet]. Open Journal of Blood Diseases. 2013 ; 3( 1): 57-61.[citado 2024 maio 11 ] Available from: https://doi.org/10.4236/ojbd.2013.31012