Filtros : "Peng, Minshi" Limpar

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  • Source: Nature Genetics. Unidade: IB

    Subjects: TRANSTORNO AUTÍSTICO, DOENÇAS GENÉTICAS, DOENÇAS DO SISTEMA NERVOSO, GENOMAS

    Acesso à fonteDOIHow to cite
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    • ABNT

      FU, Jack M et al. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, v. 54, p. 1320–1331, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41588-022-01104-0. Acesso em: 27 abr. 2024.
    • APA

      Fu, J. M., Satterstrom, F. K., Peng, M., & Passos-Bueno, M. R. (2022). Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, 54, 1320–1331. doi:10.1038/s41588-022-01104-0
    • NLM

      Fu JM, Satterstrom FK, Peng M, Passos-Bueno MR. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism [Internet]. Nature Genetics. 2022 ; 54 1320–1331.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1038/s41588-022-01104-0
    • Vancouver

      Fu JM, Satterstrom FK, Peng M, Passos-Bueno MR. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism [Internet]. Nature Genetics. 2022 ; 54 1320–1331.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1038/s41588-022-01104-0

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