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Filtros : "Guion Almeida, Maria Leine" Limpar

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  • Artigo de periodico

    Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7 (2012)

    Zechi-Ceide, Roseli Maria ; Rodrigues, Melina Guerreiro; Jehee, Fernanda Sarquis; Nakata, Nancy Mizue Kokitsu ; Passos-Bueno, Maria Rita ; Guion Almeida, Maria Leine

    Source: American Journal of Medical Genetics Part A. Unidades: HRAC, IB

    Subjects: CROMOSSOMOS, GENÉTICA MÉDICA, GENES

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

    • ABNT

      ZECHI-CEIDE, Roseli Maria et al. Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7. American Journal of Medical Genetics Part A, v. 158A, n. 7, p. 1680\20131685, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.35367. Acesso em: 28 abr. 2024.

    • APA

      Zechi-Ceide, R. M., Rodrigues, M. G., Jehee, F. S., Nakata, N. M. K., Passos-Bueno, M. R., & Guion Almeida, M. L. (2012). Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7. American Journal of Medical Genetics Part A, 158A( 7), 1680\20131685. doi:10.1002/ajmg.a.35367

    • NLM

      Zechi-Ceide RM, Rodrigues MG, Jehee FS, Nakata NMK, Passos-Bueno MR, Guion Almeida ML. Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7 [Internet]. American Journal of Medical Genetics Part A. 2012 ; 158A( 7): 1680\20131685.[citado 2024 abr. 28 ] Available from: https://doi.org/10.1002/ajmg.a.35367

    • Vancouver

      Zechi-Ceide RM, Rodrigues MG, Jehee FS, Nakata NMK, Passos-Bueno MR, Guion Almeida ML. Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7 [Internet]. American Journal of Medical Genetics Part A. 2012 ; 158A( 7): 1680\20131685.[citado 2024 abr. 28 ] Available from: https://doi.org/10.1002/ajmg.a.35367

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

    • 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: 28 abr. 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 abr. 28 ] 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 abr. 28 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x
  • 1

1 - 2 (2 records)

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