Source: American journal of human genetics. Unidade: FM
Subjects: HORMÔNIOS HIPOFISÁRIOS, MUTAÇÃO GENÉTICA, HORMÔNIO DO CRESCIMENTO
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GERGICS, Peter et al. High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency. American journal of human genetics, v. 108, n. 8, p. 1526-1539, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2021.06.013. Acesso em: 09 nov. 2024.APA
Gergics, P., Smith, C., Bando, H., Jorge, A. A. de L., Rockstroh-lippold, D., Vishnopolska, S. A., et al. (2021). High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency. American journal of human genetics, 108( 8), 1526-1539. doi:10.1016/j.ajhg.2021.06.013NLM
Gergics P, Smith C, Bando H, Jorge AA de L, Rockstroh-lippold D, Vishnopolska SA, Castinetti F, Maksutova M, Carvalho LRS, Mendonca BB de. High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency [Internet]. American journal of human genetics. 2021 ; 108( 8): 1526-1539.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.ajhg.2021.06.013Vancouver
Gergics P, Smith C, Bando H, Jorge AA de L, Rockstroh-lippold D, Vishnopolska SA, Castinetti F, Maksutova M, Carvalho LRS, Mendonca BB de. High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency [Internet]. American journal of human genetics. 2021 ; 108( 8): 1526-1539.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.ajhg.2021.06.013