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Filtros : "Reino Unido" "2008" "Clinical Dysmorphology" Removidos: "PEREIRA, SAYONARA SOUSA" "SILVA, DILMA DE MELO" "1969" Limpar

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  • Artigo de periodico

    Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder (2008)

    Guion-Almeida, Maria Leine; Richieri-Costa, Antonio; Ceide, Roseli Maria Zechi

    Source: Clinical Dysmorphology. Unidade: HRAC

    Subjects: HOLOPROSENCEFALIA, ANORMALIDADES CRANIOFACIAIS

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

    • ABNT

      GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio e CEIDE, Roseli Maria Zechi. Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder. Clinical Dysmorphology, v. 17, n. Ja 2008, p. 41-46, 2008Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e328274244f. Acesso em: 08 set. 2024.

    • APA

      Guion-Almeida, M. L., Richieri-Costa, A., & Ceide, R. M. Z. (2008). Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder. Clinical Dysmorphology, 17( Ja 2008), 41-46. doi:10.1097/mcd.0b013e328274244f

    • NLM

      Guion-Almeida ML, Richieri-Costa A, Ceide RMZ. Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder [Internet]. Clinical Dysmorphology. 2008 ; 17( Ja 2008): 41-46.[citado 2024 set. 08 ] Available from: https://doi.org/10.1097/mcd.0b013e328274244f

    • Vancouver

      Guion-Almeida ML, Richieri-Costa A, Ceide RMZ. Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder [Internet]. Clinical Dysmorphology. 2008 ; 17( Ja 2008): 41-46.[citado 2024 set. 08 ] Available from: https://doi.org/10.1097/mcd.0b013e328274244f

  • Artigo de periodico

    Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? (2008)

    Richieri-Costa, Antonio; Ceide, Roseli Maria Zechi; Guion-Almeida, Maria Leine

    Source: Clinical Dysmorphology. Unidade: HRAC

    Subjects: ANORMALIDADES MÚLTIPLAS, TERATOMA, ANORMALIDADES CARDIOVASCULARES, NEOPLASIAS BUCAIS

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

    • ABNT

      RICHIERI-COSTA, Antonio e CEIDE, Roseli Maria Zechi e GUION-ALMEIDA, Maria Leine. Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity?. Clinical Dysmorphology, v. 17, n. 2, p. 149-150, 2008Tradução . . Disponível em: https://doi.org/10.1097/MCD.0b013e3282f254b7. Acesso em: 08 set. 2024.

    • APA

      Richieri-Costa, A., Ceide, R. M. Z., & Guion-Almeida, M. L. (2008). Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? Clinical Dysmorphology, 17( 2), 149-150. doi:10.1097/MCD.0b013e3282f254b7

    • NLM

      Richieri-Costa A, Ceide RMZ, Guion-Almeida ML. Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? [Internet]. Clinical Dysmorphology. 2008 ; 17( 2): 149-150.[citado 2024 set. 08 ] Available from: https://doi.org/10.1097/MCD.0b013e3282f254b7

    • Vancouver

      Richieri-Costa A, Ceide RMZ, Guion-Almeida ML. Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? [Internet]. Clinical Dysmorphology. 2008 ; 17( 2): 149-150.[citado 2024 set. 08 ] Available from: https://doi.org/10.1097/MCD.0b013e3282f254b7

  • Artigo de periodico

    Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene (2008)

    Ceide, Roseli Maria Zechi; Oliveira, Nélio Alessandro de Jesus; Guion-Almeida, Maria Leine; Antunes, Luis Fernando Benedito Bergami; Richieri-Costa, Antonio; Passos-Bueno, Maria Rita

    Source: Clinical Dysmorphology. Unidades: HRAC, IB

    Subjects: ANORMALIDADES MÚLTIPLAS, FENÓTIPOS, GENES

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

    • ABNT

      CEIDE, Roseli Maria Zechi et al. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene. Clinical Dysmorphology, v. 17, n. 3, p. 225-226, 2008Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e3282fe1b8e. Acesso em: 08 set. 2024.

    • APA

      Ceide, R. M. Z., Oliveira, N. A. de J., Guion-Almeida, M. L., Antunes, L. F. B. B., Richieri-Costa, A., & Passos-Bueno, M. R. (2008). Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene. Clinical Dysmorphology, 17( 3), 225-226. doi:10.1097/mcd.0b013e3282fe1b8e

    • NLM

      Ceide RMZ, Oliveira NA de J, Guion-Almeida ML, Antunes LFBB, Richieri-Costa A, Passos-Bueno MR. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene [Internet]. Clinical Dysmorphology. 2008 ; 17( 3): 225-226.[citado 2024 set. 08 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e

    • Vancouver

      Ceide RMZ, Oliveira NA de J, Guion-Almeida ML, Antunes LFBB, Richieri-Costa A, Passos-Bueno MR. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene [Internet]. Clinical Dysmorphology. 2008 ; 17( 3): 225-226.[citado 2024 set. 08 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e
  • 1

1 - 3 (3 records)

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