Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
ABNT
RABBI-BORTOLINI, Eliete et al. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis. American Journal of Medical Genetics, v. 76, p. 288-290, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q. Acesso em: 02 maio 2024.APA
Rabbi-Bortolini, E., Bernardino, A. L. F., Lopes, A. L., Ferri, A. da S., Passos-Bueno, M. R., & Zatz, M. (1998). Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis. American Journal of Medical Genetics, 76, 288-290. doi:10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-qNLM
Rabbi-Bortolini E, Bernardino ALF, Lopes AL, Ferri A da S, Passos-Bueno MR, Zatz M. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis [Internet]. American Journal of Medical Genetics. 1998 ; 76 288-290.[citado 2024 maio 02 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-qVancouver
Rabbi-Bortolini E, Bernardino ALF, Lopes AL, Ferri A da S, Passos-Bueno MR, Zatz M. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis [Internet]. American Journal of Medical Genetics. 1998 ; 76 288-290.[citado 2024 maio 02 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q