Source: Journal of Oral Diagnosis. Unidade: FOB
Subjects: ENVELHECIMENTO CELULAR, MANIFESTAÇÕES BUCAIS, ERROS INATOS DO METABOLISMO
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NOGUEIRA, Alexandre Simões et al. Hutchinson-Gilford Progeria Syndrome (HGPS): relevant aspects of a rare syndrome diagnosed in a Brazilian child. Journal of Oral Diagnosis, v. 1, n. 2, p. 91-98, 2012Tradução . . Disponível em: https://doi.org/10.5935/2525-5711.20160009. Acesso em: 04 set. 2024.APA
Nogueira, A. S., Nogueira, C. B. P., Medeiros, R., Beviláqua, A. C., Santos, P. S. da S., Bullen, I. R. F. R., & Gonçales, E. S. (2012). Hutchinson-Gilford Progeria Syndrome (HGPS): relevant aspects of a rare syndrome diagnosed in a Brazilian child. Journal of Oral Diagnosis, 1( 2), 91-98. doi:10.5935/2525-5711.20160009NLM
Nogueira AS, Nogueira CBP, Medeiros R, Beviláqua AC, Santos PS da S, Bullen IRFR, Gonçales ES. Hutchinson-Gilford Progeria Syndrome (HGPS): relevant aspects of a rare syndrome diagnosed in a Brazilian child [Internet]. Journal of Oral Diagnosis. 2012 ; 1( 2): 91-98.[citado 2024 set. 04 ] Available from: https://doi.org/10.5935/2525-5711.20160009Vancouver
Nogueira AS, Nogueira CBP, Medeiros R, Beviláqua AC, Santos PS da S, Bullen IRFR, Gonçales ES. Hutchinson-Gilford Progeria Syndrome (HGPS): relevant aspects of a rare syndrome diagnosed in a Brazilian child [Internet]. Journal of Oral Diagnosis. 2012 ; 1( 2): 91-98.[citado 2024 set. 04 ] Available from: https://doi.org/10.5935/2525-5711.20160009