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Filtros : "Indexado no Index Medicus" "Indexado no Science Citation Index" "HRAC" Removidos: "FEP" "Vessoni Penna, Thereza Christina" Limpar

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1 - 4 (4 records)

  • Artigo de periodico

    Nonprogressive congenital cerebellar ataxia, iris heterochromia, mental retardation and language impairment in two brothers (2010)

    Lamônica, Dionísia Aparecida Cusin; Maximino, Luciana Paula; Abramides, Dagma Venturini Marques; Souza, Deise H.; Richieri-Costa, Antonio

    Source: Clinical Dysmorphology. Unidades: FOB, HRAC

    Subjects: RETARDO MENTAL (PATOLOGIA), TRANSTORNOS DA LINGUAGEM INFANTIL, DOENÇAS HEREDITÁRIAS, DOENÇAS CEREBRAIS

    Acesso à fonteDOIHow to cite
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    • ABNT

      LAMÔNICA, Dionísia Aparecida Cusin et al. Nonprogressive congenital cerebellar ataxia, iris heterochromia, mental retardation and language impairment in two brothers. Clinical Dysmorphology, v. 19, n. 2, p. 76-78, 2010Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e32833034fc. Acesso em: 08 jul. 2024.

    • APA

      Lamônica, D. A. C., Maximino, L. P., Abramides, D. V. M., Souza, D. H., & Richieri-Costa, A. (2010). Nonprogressive congenital cerebellar ataxia, iris heterochromia, mental retardation and language impairment in two brothers. Clinical Dysmorphology, 19( 2), 76-78. doi:10.1097/mcd.0b013e32833034fc

    • NLM

      Lamônica DAC, Maximino LP, Abramides DVM, Souza DH, Richieri-Costa A. Nonprogressive congenital cerebellar ataxia, iris heterochromia, mental retardation and language impairment in two brothers [Internet]. Clinical Dysmorphology. 2010 ; 19( 2): 76-78.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1097/mcd.0b013e32833034fc

    • Vancouver

      Lamônica DAC, Maximino LP, Abramides DVM, Souza DH, Richieri-Costa A. Nonprogressive congenital cerebellar ataxia, iris heterochromia, mental retardation and language impairment in two brothers [Internet]. Clinical Dysmorphology. 2010 ; 19( 2): 76-78.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1097/mcd.0b013e32833034fc

  • Artigo de periodico

    Longitudinal study of the growth of infants with isolated Robin sequence considered being severe cases (2008)

    Marques, Ilza Lazarini; Bettiol, Heloisa; Souza, Luiz de; Barbieri, Marco Antonio; Bachega, Maria Irene

    Source: Acta Paediatrica. Unidades: HRAC, FMRP

    Assunto: SÍNDROME DE PIERRE ROBIN

    Acesso à fonteDOIHow to cite
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    • ABNT

      MARQUES, Ilza Lazarini et al. Longitudinal study of the growth of infants with isolated Robin sequence considered being severe cases. Acta Paediatrica, v. 97, n. 3, p. 371-375, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1651-2227.2008.00664.x. Acesso em: 08 jul. 2024.

    • APA

      Marques, I. L., Bettiol, H., Souza, L. de, Barbieri, M. A., & Bachega, M. I. (2008). Longitudinal study of the growth of infants with isolated Robin sequence considered being severe cases. Acta Paediatrica, 97( 3), 371-375. doi:10.1111/j.1651-2227.2008.00664.x

    • NLM

      Marques IL, Bettiol H, Souza L de, Barbieri MA, Bachega MI. Longitudinal study of the growth of infants with isolated Robin sequence considered being severe cases [Internet]. Acta Paediatrica. 2008 ; 97( 3): 371-375.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1111/j.1651-2227.2008.00664.x

    • Vancouver

      Marques IL, Bettiol H, Souza L de, Barbieri MA, Bachega MI. Longitudinal study of the growth of infants with isolated Robin sequence considered being severe cases [Internet]. Acta Paediatrica. 2008 ; 97( 3): 371-375.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1111/j.1651-2227.2008.00664.x

  • Artigo de periodico

    A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate (2006)

    Guion-Almeida, Maria Leine; Ceide, Roseli Maria Zechi; Vendramini, Siulan; Tabith Junior, Alfredo

    Source: Clinical Dysmorphology. Unidade: HRAC

    Subjects: ANORMALIDADES CRANIOFACIAIS, FISSURA PALATINA

    Acesso à fonteDOIHow to cite
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    • ABNT

      GUION-ALMEIDA, Maria Leine et al. A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate. Clinical Dysmorphology, v. 15, n. 3, p. 171-174, 2006Tradução . . Disponível em: https://doi.org/10.1097/01.mcd.0000220603.09661.7e. Acesso em: 08 jul. 2024.

    • APA

      Guion-Almeida, M. L., Ceide, R. M. Z., Vendramini, S., & Tabith Junior, A. (2006). A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate. Clinical Dysmorphology, 15( 3), 171-174. doi:10.1097/01.mcd.0000220603.09661.7e

    • NLM

      Guion-Almeida ML, Ceide RMZ, Vendramini S, Tabith Junior A. A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate [Internet]. Clinical Dysmorphology. 2006 ; 15( 3): 171-174.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1097/01.mcd.0000220603.09661.7e

    • Vancouver

      Guion-Almeida ML, Ceide RMZ, Vendramini S, Tabith Junior A. A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate [Internet]. Clinical Dysmorphology. 2006 ; 15( 3): 171-174.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1097/01.mcd.0000220603.09661.7e

  • Artigo de periodico

    Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome (2002)

    Sandrin Garcia, P; Macedo, C; Martelli, Lúcia Regina; Ramos, Ester Silveira; Guion Almeida, Maria Leine; Richieri Costa, Antônio; Passos, Geraldo Aleixo Silva

    Source: Clinical genetics. Unidades: FMRP, HRAC, FORP

    Subjects: GENÉTICA, DNA

    Acesso à fonteDOIHow to cite
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    • ABNT

      SANDRIN GARCIA, P et al. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clinical genetics, v. 61, n. 5, p. 380-383, 2002Tradução . . Disponível em: https://doi.org/10.1034/j.1399-0004.2002.610511.x. Acesso em: 08 jul. 2024.

    • APA

      Sandrin Garcia, P., Macedo, C., Martelli, L. R., Ramos, E. S., Guion Almeida, M. L., Richieri Costa, A., & Passos, G. A. S. (2002). Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clinical genetics, 61( 5), 380-383. doi:10.1034/j.1399-0004.2002.610511.x

    • NLM

      Sandrin Garcia P, Macedo C, Martelli LR, Ramos ES, Guion Almeida ML, Richieri Costa A, Passos GAS. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome [Internet]. Clinical genetics. 2002 ; 61( 5): 380-383.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x

    • Vancouver

      Sandrin Garcia P, Macedo C, Martelli LR, Ramos ES, Guion Almeida ML, Richieri Costa A, Passos GAS. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome [Internet]. Clinical genetics. 2002 ; 61( 5): 380-383.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x
  • 1

1 - 4 (4 records)

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