Filtros : "HRAC" "2004" Removidos: "Brasil" "ERUPÇÃO DENTÁRIA" 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: 16 abr. 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 abr. 16 ]
    • 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 abr. 16 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: ANORMALIDADES MÚLTIPLAS

    Acesso à fonteDOIHow to cite
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    • ABNT

      GUION-ALMEIDA, Maria Leine e PAULA, Ligiane Alves Machado e RICHIERI-COSTA, Antonio. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome?. American Journal of Medical Genetics, v. 129A, n. 2, p. 156-161, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30153. Acesso em: 16 abr. 2024.
    • APA

      Guion-Almeida, M. L., Paula, L. A. M., & Richieri-Costa, A. (2004). Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? American Journal of Medical Genetics, 129A( 2), 156-161. doi:10.1002/ajmg.a.30153
    • NLM

      Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? [Internet]. American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1002/ajmg.a.30153
    • Vancouver

      Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? [Internet]. American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1002/ajmg.a.30153
  • Source: Journal of Clinical Pediatric Dentistry. Unidade: HRAC

    Subjects: DENTIÇÃO MISTA, ORTODONTIA INTERCEPTORA, MOVIMENTAÇÃO DENTÁRIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      SILVA FILHO, Omar Gabriel da et al. Behavior of partially formed roots of teeth submitted to orthodontic movement. Journal of Clinical Pediatric Dentistry, v. 28, n. 2, p. 147-154, 2004Tradução . . Disponível em: https://doi.org/10.17796/jcpd.28.2.56n643558770p763. Acesso em: 16 abr. 2024.
    • APA

      Silva Filho, O. G. da, Mendes, O. de F., Ozawa, T. O., Ferrari Junior, F. M., & Corrêa, T. M. (2004). Behavior of partially formed roots of teeth submitted to orthodontic movement. Journal of Clinical Pediatric Dentistry, 28( 2), 147-154. doi:10.17796/jcpd.28.2.56n643558770p763
    • NLM

      Silva Filho OG da, Mendes O de F, Ozawa TO, Ferrari Junior FM, Corrêa TM. Behavior of partially formed roots of teeth submitted to orthodontic movement [Internet]. Journal of Clinical Pediatric Dentistry. 2004 ; 28( 2): 147-154.[citado 2024 abr. 16 ] Available from: https://doi.org/10.17796/jcpd.28.2.56n643558770p763
    • Vancouver

      Silva Filho OG da, Mendes O de F, Ozawa TO, Ferrari Junior FM, Corrêa TM. Behavior of partially formed roots of teeth submitted to orthodontic movement [Internet]. Journal of Clinical Pediatric Dentistry. 2004 ; 28( 2): 147-154.[citado 2024 abr. 16 ] Available from: https://doi.org/10.17796/jcpd.28.2.56n643558770p763
  • Source: Journal of Neuroradiologie. Unidades: HRAC, FM

    Subjects: ANORMALIDADES CRANIOFACIAIS, CÉREBRO

    Acesso à fonteDOIHow to cite
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    • ABNT

      FERNANDES, Adriano Yacubian et al. Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment. Journal of Neuroradiologie, v. 31, n. 2, p. 116-122, 2004Tradução . . Disponível em: https://doi.org/10.1016/s0150-9861(04)96978-7. Acesso em: 16 abr. 2024.
    • APA

      Fernandes, A. Y., Palhares Neto, A., Giglio, A., Gabarra, R. C., Zanini, S. A., Portela, L., & Plese, J. P. P. (2004). Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment. Journal of Neuroradiologie, 31( 2), 116-122. doi:10.1016/s0150-9861(04)96978-7
    • NLM

      Fernandes AY, Palhares Neto A, Giglio A, Gabarra RC, Zanini SA, Portela L, Plese JPP. Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment [Internet]. Journal of Neuroradiologie. 2004 ; 31( 2): 116-122.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1016/s0150-9861(04)96978-7
    • Vancouver

      Fernandes AY, Palhares Neto A, Giglio A, Gabarra RC, Zanini SA, Portela L, Plese JPP. Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment [Internet]. Journal of Neuroradiologie. 2004 ; 31( 2): 116-122.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1016/s0150-9861(04)96978-7

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