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Filtros : "MALFORMAÇÕES" "SÍNDROME DE ANGELMAN" "KOIFFMANN, CELIA PRISZKULNIK" Removido: "Rosenberg, Carla" Limpar

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  • Artigo de periodico

    Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome (2000)

    Fridman, Cintia; Koiffmann, Celia Priszkulnik

    Source: American Journal of Medical Genetics. Unidade: IB

    Subjects: GENÉTICA MÉDICA, MALFORMAÇÕES, SÍNDROME DE ANGELMAN

    Acesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      FRIDMAN, Cintia e KOIFFMANN, Celia Priszkulnik. Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome. American Journal of Medical Genetics, v. 94, p. 249-253, 2000Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(20000918)94:3%3C249::aid-ajmg12%3E3.0.co;2-x. Acesso em: 02 out. 2024.

    • APA

      Fridman, C., & Koiffmann, C. P. (2000). Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome. American Journal of Medical Genetics, 94, 249-253. doi:10.1002/1096-8628(20000918)94:3%3C249::aid-ajmg12%3E3.0.co;2-x

    • NLM

      Fridman C, Koiffmann CP. Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome [Internet]. American Journal of Medical Genetics. 2000 ; 94 249-253.[citado 2024 out. 02 ] Available from: https://doi.org/10.1002/1096-8628(20000918)94:3%3C249::aid-ajmg12%3E3.0.co;2-x

    • Vancouver

      Fridman C, Koiffmann CP. Origin of uniparental disomy 15 in patients with Prader-Willi or Algelman Syndrome [Internet]. American Journal of Medical Genetics. 2000 ; 94 249-253.[citado 2024 out. 02 ] Available from: https://doi.org/10.1002/1096-8628(20000918)94:3%3C249::aid-ajmg12%3E3.0.co;2-x

  • Artigo de periodico

    Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes (2000)

    Fridman, Cintia; Koiffmann, Celia Priszkulnik

    Source: Genetics and Molecular Biology. Unidade: IB

    Subjects: GENÉTICA MÉDICA, MALFORMAÇÕES, SÍNDROME DE ANGELMAN, EXPRESSÃO GÊNICA, FENÓTIPOS (ASPECTOS MÉDICOS)

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

    • ABNT

      FRIDMAN, Cintia e KOIFFMANN, Celia Priszkulnik. Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes. Genetics and Molecular Biology, v. 23, n. 4, p. 715-724, 2000Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572000000400004. Acesso em: 02 out. 2024.

    • APA

      Fridman, C., & Koiffmann, C. P. (2000). Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes. Genetics and Molecular Biology, 23( 4), 715-724. doi:10.1590/s1415-47572000000400004

    • NLM

      Fridman C, Koiffmann CP. Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes [Internet]. Genetics and Molecular Biology. 2000 ; 23( 4): 715-724.[citado 2024 out. 02 ] Available from: https://doi.org/10.1590/s1415-47572000000400004

    • Vancouver

      Fridman C, Koiffmann CP. Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes [Internet]. Genetics and Molecular Biology. 2000 ; 23( 4): 715-724.[citado 2024 out. 02 ] Available from: https://doi.org/10.1590/s1415-47572000000400004
  • 1

1 - 2 (2 records)

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