Source: American Journal of Medical Genetics Part A. Unidades: FOB, HRAC
Subjects: GENÉTICA MÉDICA, GAGUEIRA
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ABNT
PETRIN, Aline L. et al. Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case. American Journal of Medical Genetics Part A, v. 152A, n. 12, p. 3164-3172, 2010Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.33749. Acesso em: 04 jun. 2024.APA
Petrin, A. L., Giacheti, C. M., Maximino, L. P., Abramides, D. V. M., Zanchetta, S., Rossi, N. F., et al. (2010). Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case. American Journal of Medical Genetics Part A, 152A( 12), 3164-3172. doi:10.1002/ajmg.a.33749NLM
Petrin AL, Giacheti CM, Maximino LP, Abramides DVM, Zanchetta S, Rossi NF, Richieri-Costa A, Murray JC. Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case [Internet]. American Journal of Medical Genetics Part A. 2010 ; 152A( 12): 3164-3172.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1002/ajmg.a.33749Vancouver
Petrin AL, Giacheti CM, Maximino LP, Abramides DVM, Zanchetta S, Rossi NF, Richieri-Costa A, Murray JC. Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case [Internet]. American Journal of Medical Genetics Part A. 2010 ; 152A( 12): 3164-3172.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1002/ajmg.a.33749
