Torres, William Bertani 
; Lezirovitz, Karina ; Coutinho, Danillo Alencar ; Pardono, Eliete; Costa, Silvia Souza da; Antunes, Larissa do Nascimento; Oliveira, Judite de; Otto, Paulo A ; Pingault, Véronique ; Mingroni Netto, Regina Celia
Source: Audiology Research. Unidade: IB
Subjects: PERDA AUDITIVA, SURDEZ, GENÉTICA MOLECULAR, MUTAÇÃO GENÉTICA, PIGMENTOS
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ABNT
TORRES, William Bertani et al. Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants. Audiology Research, v. 14, n. 1, p. 9-25, 2024Tradução . . Disponível em: https://doi.org/10.3390/audiolres14010002. Acesso em: 04 nov. 2024.APA
Torres, W. B., Lezirovitz, K., Coutinho, D. A., Pardono, E., Costa, S. S. da, Antunes, L. do N., et al. (2024). Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants. Audiology Research, 14( 1), 9-25. doi:10.3390/audiolres14010002NLM
Torres WB, Lezirovitz K, Coutinho DA, Pardono E, Costa SS da, Antunes L do N, Oliveira J de, Otto PA, Pingault V, Mingroni Netto RC. Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants [Internet]. Audiology Research. 2024 ; 14( 1): 9-25.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/audiolres14010002Vancouver
Torres WB, Lezirovitz K, Coutinho DA, Pardono E, Costa SS da, Antunes L do N, Oliveira J de, Otto PA, Pingault V, Mingroni Netto RC. Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants [Internet]. Audiology Research. 2024 ; 14( 1): 9-25.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/audiolres14010002
