Filtros : "Indexado no ASCA" "Passos-Bueno, Maria Rita" Removido: "Pesquisa FAPESP" Limpar

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  • Source: Human Mutation. 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

      SPLENDORE, Alessandra et al. High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes. Human Mutation, v. 16, p. 315-322, 2000Tradução . . Disponível em: https://doi.org/10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-h. Acesso em: 10 nov. 2024.
    • APA

      Splendore, A., Silva, E. O. da, Alonso, L. G., Richieri-Costa, A., Alonso, N., Rosa, A., et al. (2000). High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes. Human Mutation, 16, 315-322. doi:10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-h
    • NLM

      Splendore A, Silva EO da, Alonso LG, Richieri-Costa A, Alonso N, Rosa A, Carakushansky G, Cavalcanti DP, Brunoni D, Passos-Bueno MR. High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes [Internet]. Human Mutation. 2000 ; 16 315-322.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-h
    • Vancouver

      Splendore A, Silva EO da, Alonso LG, Richieri-Costa A, Alonso N, Rosa A, Carakushansky G, Cavalcanti DP, Brunoni D, Passos-Bueno MR. High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes [Internet]. Human Mutation. 2000 ; 16 315-322.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-h
  • Source: American Journal of Medical Genetics. Unidade: IB

    Subjects: GENÉTICA MÉDICA, DISTROFIA MUSCULAR

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

      EGGERS, Sabine et al. Genetic counseling for childless women at risk for Duchenne muscular dystrophy. American Journal of Medical Genetics, v. 86, p. 447-453, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p. Acesso em: 10 nov. 2024.
    • APA

      Eggers, S., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (1999). Genetic counseling for childless women at risk for Duchenne muscular dystrophy. American Journal of Medical Genetics, 86, 447-453. doi:10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
    • NLM

      Eggers S, Pavanello R de CM, Passos-Bueno MR, Zatz M. Genetic counseling for childless women at risk for Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1999 ; 86 447-453.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
    • Vancouver

      Eggers S, Pavanello R de CM, Passos-Bueno MR, Zatz M. Genetic counseling for childless women at risk for Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1999 ; 86 447-453.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p

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