Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis (1998)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- DOI: 10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Source:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v. 76, p. 288-290, 1998
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RABBI-BORTOLINI, Eliete; BERNARDINO, Andréa L F; LOPES, Adoris L; 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[S.l.], v. 76, p. 288-290, 1998. DOI: 10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q. -
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-q -
NLM
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. American Journal of Medical Genetics. 1998 ; 76 288-290. -
Vancouver
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. American Journal of Medical Genetics. 1998 ; 76 288-290. - Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
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Informações sobre o DOI: 10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q (Fonte: oaDOI API)
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