Filtros : "Marçano, Ana Carolina Braga" 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: 24 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. 24 ]
    • 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. 24 ]
  • Source: Programme & Abstracts. Conference titles: International Congress on Cleft Palate and Related Craniofacial Anomalies. Unidade: HRAC

    Subjects: ANOMALIA CRANIOFACIAL, FISSURA LÁBIOPALATINA

    Versão PublicadaHow to cite
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    • ABNT

      RICHIERI-COSTA, Antonio e MARÇANO, Ana Carolina Braga e GUION-ALMEIDA, Maria Leine. Atypical craniofacial clefts: a syndromological approach. 2001, Anais.. Goteborg: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2001. Disponível em: https://repositorio.usp.br/directbitstream/cd2b644c-b5c8-4aa3-86e9-cd8536ae3c9d/3167181.pdf. Acesso em: 24 abr. 2024.
    • APA

      Richieri-Costa, A., Marçano, A. C. B., & Guion-Almeida, M. L. (2001). Atypical craniofacial clefts: a syndromological approach. In Programme & Abstracts. Goteborg: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/cd2b644c-b5c8-4aa3-86e9-cd8536ae3c9d/3167181.pdf
    • NLM

      Richieri-Costa A, Marçano ACB, Guion-Almeida ML. Atypical craniofacial clefts: a syndromological approach [Internet]. Programme & Abstracts. 2001 ;[citado 2024 abr. 24 ] Available from: https://repositorio.usp.br/directbitstream/cd2b644c-b5c8-4aa3-86e9-cd8536ae3c9d/3167181.pdf
    • Vancouver

      Richieri-Costa A, Marçano ACB, Guion-Almeida ML. Atypical craniofacial clefts: a syndromological approach [Internet]. Programme & Abstracts. 2001 ;[citado 2024 abr. 24 ] Available from: https://repositorio.usp.br/directbitstream/cd2b644c-b5c8-4aa3-86e9-cd8536ae3c9d/3167181.pdf
  • Source: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. Unidade: HRAC

    Subjects: GENÉTICA, GENÉTICA MÉDICA

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

      MARÇANO, Ana Carolina Braga e RICHIERI-COSTA, Antonio. A newly recognized autosomal dominant mandibulofacaial dysostosis (Bauru type): report on a Brazilian family. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, v. 1, n. ja 1998, p. 37-41, 1998Tradução . . Acesso em: 24 abr. 2024.
    • APA

      Marçano, A. C. B., & Richieri-Costa, A. (1998). A newly recognized autosomal dominant mandibulofacaial dysostosis (Bauru type): report on a Brazilian family. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 1( ja 1998), 37-41.
    • NLM

      Marçano ACB, Richieri-Costa A. A newly recognized autosomal dominant mandibulofacaial dysostosis (Bauru type): report on a Brazilian family. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1998 ; 1( ja 1998): 37-41.[citado 2024 abr. 24 ]
    • Vancouver

      Marçano ACB, Richieri-Costa A. A newly recognized autosomal dominant mandibulofacaial dysostosis (Bauru type): report on a Brazilian family. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1998 ; 1( ja 1998): 37-41.[citado 2024 abr. 24 ]

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