Filtros : "Indexado na Base de Dados Medline" "Estados Unidos" "HRAC" Removido: "GENÉTICA" Limpar

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  • Source: Journal of Medical Genetics. Unidade: HRAC

    Subjects: MUTAÇÃO GENÉTICA, FISSURA PALATINA

    How to cite
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    • ABNT

      MARÇANO, Ana Carolina Braga et al. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics, v. 41, n. Ja 2004, p. 68-74, 2004Tradução . . Acesso em: 30 set. 2024.
    • APA

      Marçano, A. C. B., Doudney, K., Braybrook, C., Squires, R., Patton, M. A., Lees, M. M., et al. (2004). TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics, 41( Ja 2004), 68-74.
    • NLM

      Marçano ACB, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics. 2004 ; 41( Ja 2004): 68-74.[citado 2024 set. 30 ]
    • Vancouver

      Marçano ACB, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics. 2004 ; 41( Ja 2004): 68-74.[citado 2024 set. 30 ]
  • Source: Nature Genetics. Unidade: HRAC

    Subjects: MUTAÇÃO GENÉTICA, GENES, FISSURA LÁBIOPALATINA

    Acesso à fonteDOIHow to cite
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    • ABNT

      SUZUKI, Koji et al. Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia. Nature Genetics, v. 25, p. 427-430, 2000Tradução . . Disponível em: https://doi.org/10.1038/78119. Acesso em: 30 set. 2024.
    • APA

      Suzuki, K., Hu, D., Bustos, T., Zlotogora, J., Richieri-Costa, A., Helms, J. A., & Spritz, R. A. (2000). Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia. Nature Genetics, 25, 427-430. doi:10.1038/78119
    • NLM

      Suzuki K, Hu D, Bustos T, Zlotogora J, Richieri-Costa A, Helms JA, Spritz RA. Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia [Internet]. Nature Genetics. 2000 ; 25 427-430.[citado 2024 set. 30 ] Available from: https://doi.org/10.1038/78119
    • Vancouver

      Suzuki K, Hu D, Bustos T, Zlotogora J, Richieri-Costa A, Helms JA, Spritz RA. Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia [Internet]. Nature Genetics. 2000 ; 25 427-430.[citado 2024 set. 30 ] Available from: https://doi.org/10.1038/78119
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subjects: ANORMALIDADES MÚLTIPLAS, GENÉTICA MÉDICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      RICHIERI-COSTA, Antonio e GORLIN, Robert J. Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity. American Journal of Medical Genetics, v. No 1994, n. 3, p. 222-226, 1994Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320530305. Acesso em: 30 set. 2024.
    • APA

      Richieri-Costa, A., & Gorlin, R. J. (1994). Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity. American Journal of Medical Genetics, No 1994( 3), 222-226. doi:10.1002/ajmg.1320530305
    • NLM

      Richieri-Costa A, Gorlin RJ. Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity [Internet]. American Journal of Medical Genetics. 1994 ; No 1994( 3): 222-226.[citado 2024 set. 30 ] Available from: https://doi.org/10.1002/ajmg.1320530305
    • Vancouver

      Richieri-Costa A, Gorlin RJ. Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity [Internet]. American Journal of Medical Genetics. 1994 ; No 1994( 3): 222-226.[citado 2024 set. 30 ] Available from: https://doi.org/10.1002/ajmg.1320530305

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