Filtros : "Ott, J" Limpar

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  • Source: American Journal of Medical Genetics. Unidade: IB

    Assunto: GENÉTICA MÉDICA

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

      PASSOS-BUENO, Maria Rita et al. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (lgmd) and 6q probes flanking the dystrophin-related sequence. American Journal of Medical Genetics, v. 38, n. ja 1991, p. 140-6, 1991Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320380130. Acesso em: 10 out. 2024.
    • APA

      Passos-Bueno, M. R., Terwilliger, J., Ott, J., Vainzof, M., Love, D. R., Davies, K. E., & Zatz, M. (1991). Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (lgmd) and 6q probes flanking the dystrophin-related sequence. American Journal of Medical Genetics, 38( ja 1991), 140-6. doi:10.1002/ajmg.1320380130
    • NLM

      Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (lgmd) and 6q probes flanking the dystrophin-related sequence [Internet]. American Journal of Medical Genetics. 1991 ;38( ja 1991): 140-6.[citado 2024 out. 10 ] Available from: https://doi.org/10.1002/ajmg.1320380130
    • Vancouver

      Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (lgmd) and 6q probes flanking the dystrophin-related sequence [Internet]. American Journal of Medical Genetics. 1991 ;38( ja 1991): 140-6.[citado 2024 out. 10 ] Available from: https://doi.org/10.1002/ajmg.1320380130
  • Source: Journal of the Neurological Sciences. Unidade: IB

    Assunto: GENÉTICA MÉDICA

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

      PASSOS-BUENO, Maria Rita et al. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27. Journal of the Neurological Sciences, v. 102, p. 206-8, 1991Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(91)90070-n. Acesso em: 10 out. 2024.
    • APA

      Passos-Bueno, M. R., Byth, B., Love, D., Terwilliger, J., Ott, J., Rapaport, D., et al. (1991). Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27. Journal of the Neurological Sciences, 102, 206-8. doi:10.1016/0022-510x(91)90070-n
    • NLM

      Passos-Bueno MR, Byth B, Love D, Terwilliger J, Ott J, Rapaport D, Vainzof M, Zatz M, Davies KE. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27 [Internet]. Journal of the Neurological Sciences. 1991 ;102 206-8.[citado 2024 out. 10 ] Available from: https://doi.org/10.1016/0022-510x(91)90070-n
    • Vancouver

      Passos-Bueno MR, Byth B, Love D, Terwilliger J, Ott J, Rapaport D, Vainzof M, Zatz M, Davies KE. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27 [Internet]. Journal of the Neurological Sciences. 1991 ;102 206-8.[citado 2024 out. 10 ] Available from: https://doi.org/10.1016/0022-510x(91)90070-n

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