Freitas, Erika L; Oiticica, Jeanne; Silva, Amanda G; Bittar, Roseli Saraiva Moreira; Rosenberg, Carla 
; Mingroni Netto, Regina Celia
Fonte: European Journal of Medical Genetics. Unidade: IB
Assuntos: PERDA AUDITIVA HEREDITÁRIA, GENÉTICA MÉDICA, PERDA AUDITIVA NEUROSSENSORIAL, MUTAÇÃO GENÉTICA
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FREITAS, Erika L et al. Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss. European Journal of Medical Genetics, v. 57, n. 4, p. 125-128, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2014.02.006. Acesso em: 08 out. 2024.APA
Freitas, E. L., Oiticica, J., Silva, A. G., Bittar, R. S. M., Rosenberg, C., & Mingroni Netto, R. C. (2014). Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss. European Journal of Medical Genetics, 57( 4), 125-128. doi:10.1016/j.ejmg.2014.02.006NLM
Freitas EL, Oiticica J, Silva AG, Bittar RSM, Rosenberg C, Mingroni Netto RC. Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss [Internet]. European Journal of Medical Genetics. 2014 ; 57( 4): 125-128.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.ejmg.2014.02.006Vancouver
Freitas EL, Oiticica J, Silva AG, Bittar RSM, Rosenberg C, Mingroni Netto RC. Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss [Internet]. European Journal of Medical Genetics. 2014 ; 57( 4): 125-128.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.ejmg.2014.02.006
