Filtros : "Indexado na Base de Dados Medline" "Ribeiro, Lucilene Arilho" Removido: "1936" Limpar

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  • Source: Clinical Dysmorphology. Unidades: HRAC, FOB, HRACF

    Subjects: SÍNDROMES OROFACIODIGITAIS, VENTRÍCULOS CEREBRAIS, ANORMALIDADES MÚLTIPLAS

    Acesso à fonteDOIHow to cite
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    • ABNT

      CASTRO, Carlos Henrique Bettoni Cruz de et al. Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrome?. Clinical Dysmorphology, v. 14, n. 4, p. 197-201, 2005Tradução . . Disponível em: https://doi.org/10.1097/00019605-200510000-00006. Acesso em: 18 out. 2024.
    • APA

      Castro, C. H. B. C. de, Freitas, P. Z., Antoneli, M. Z., Santiago, G., Ribeiro, L. A., & Richieri-Costa, A. (2005). Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrome? Clinical Dysmorphology, 14( 4), 197-201. doi:10.1097/00019605-200510000-00006
    • NLM

      Castro CHBC de, Freitas PZ, Antoneli MZ, Santiago G, Ribeiro LA, Richieri-Costa A. Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrome? [Internet]. Clinical Dysmorphology. 2005 ; 14( 4): 197-201.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/00019605-200510000-00006
    • Vancouver

      Castro CHBC de, Freitas PZ, Antoneli MZ, Santiago G, Ribeiro LA, Richieri-Costa A. Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrome? [Internet]. Clinical Dysmorphology. 2005 ; 14( 4): 197-201.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/00019605-200510000-00006
  • Source: American Journal of Medical Genetics. Part A. Unidade: HRAC

    Subjects: ANORMALIDADES MÚLTIPLAS, HOLOPROSENCEFALIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      RICHIERI-COSTA, Antonio e RIBEIRO, Lucilene Arilho. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 352-353, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30628. Acesso em: 18 out. 2024.
    • APA

      Richieri-Costa, A., & Ribeiro, L. A. (2005). Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases. American Journal of Medical Genetics. Part A, 136( 4), 352-353. doi:10.1002/ajmg.a.30628
    • NLM

      Richieri-Costa A, Ribeiro LA. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 352-353.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30628
    • Vancouver

      Richieri-Costa A, Ribeiro LA. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 352-353.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30628
  • Source: American Journal of Medical Genetics. Part A. Unidade: HRAC

    Subjects: ANORMALIDADES MÚLTIPLAS, DESENVOLVIMENTO FÍSICO, MAXILA

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    • ABNT

      RIBEIRO, Lucilene Arilho e RICHIERI-COSTA, Antonio. Single median maxillary central incisor, hypophyseal tumor, and SHH mutation. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 346-347, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30625. Acesso em: 18 out. 2024.
    • APA

      Ribeiro, L. A., & Richieri-Costa, A. (2005). Single median maxillary central incisor, hypophyseal tumor, and SHH mutation. American Journal of Medical Genetics. Part A, 136( 4), 346-347. doi:10.1002/ajmg.a.30625
    • NLM

      Ribeiro LA, Richieri-Costa A. Single median maxillary central incisor, hypophyseal tumor, and SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 346-347.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30625
    • Vancouver

      Ribeiro LA, Richieri-Costa A. Single median maxillary central incisor, hypophyseal tumor, and SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 346-347.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30625
  • Source: American Journal of Medical Genetics. Part A. Unidade: HRAC

    Assunto: ANORMALIDADES MÚLTIPLAS

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    • ABNT

      RIBEIRO, Lucilene Arilho e RICHIERI-COSTA, Antonio. Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 348-349, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30626. Acesso em: 18 out. 2024.
    • APA

      Ribeiro, L. A., & Richieri-Costa, A. (2005). Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation. American Journal of Medical Genetics. Part A, 136( 4), 348-349. doi:10.1002/ajmg.a.30626
    • NLM

      Ribeiro LA, Richieri-Costa A. Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 348-349.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30626
    • Vancouver

      Ribeiro LA, Richieri-Costa A. Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 348-349.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30626
  • Source: American Journal of Medical Genetics. Part A. Unidade: HRAC

    Subjects: ANORMALIDADES MÚLTIPLAS, HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA

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    • ABNT

      RIBEIRO, Lucilene Arilho e GUERINI, Rita de Cássia Mecca e RICHIERI-COSTA, Antonio. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 350-351, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30627. Acesso em: 18 out. 2024.
    • APA

      Ribeiro, L. A., Guerini, R. de C. M., & Richieri-Costa, A. (2005). Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects. American Journal of Medical Genetics. Part A, 136( 4), 350-351. doi:10.1002/ajmg.a.30627
    • NLM

      Ribeiro LA, Guerini R de CM, Richieri-Costa A. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 350-351.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30627
    • Vancouver

      Ribeiro LA, Guerini R de CM, Richieri-Costa A. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 350-351.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30627

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