Subjects: MUTAÇÃO GENÉTICA, NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA), DOENÇAS GENÉTICAS, CARCINOMA, MEGACOLON (GENÉTICA), NEOPLASIAS DA TIREOIDE
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QUEDAS, Elisangela P. S. et al. RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family. Clinics, v. 67, p. 57-61, 2012Tradução . . Disponível em: https://doi.org/10.6061/clinics/2012(Sup01)11. Acesso em: 09 maio 2024.APA
Quedas, E. P. S., Toledo, R. A., Longuini, V. C., Sekiya, T., Coutinho, F. L., Toledo, S. P. A., & Tannuri, U. (2012). RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family. Clinics, 67, 57-61. doi:10.6061/clinics/2012(Sup01)11NLM
Quedas EPS, Toledo RA, Longuini VC, Sekiya T, Coutinho FL, Toledo SPA, Tannuri U. RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family [Internet]. Clinics. 2012 ; 67 57-61.[citado 2024 maio 09 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)11Vancouver
Quedas EPS, Toledo RA, Longuini VC, Sekiya T, Coutinho FL, Toledo SPA, Tannuri U. RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family [Internet]. Clinics. 2012 ; 67 57-61.[citado 2024 maio 09 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)11