Filtros : "HRAC" "American Journal of Medical Genetics" Removidos: "HRAC-SCODSAC-61" "Annual Meeting of the Brazilian Society for Dental Research - Brazilian Division of the IADR" "CARREIRA, DANIELA GAMBA GARIB" Limpar

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  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subjects: GENÉTICA, GENÉTICA MÉDICA

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      GUION-ALMEIDA, Maria Leine et al. Blepharo-cheilo-dontic (BCD) syndrome: report on four new patients. American Journal of Medical Genetics, v. 76, n. 5, p. 133-136, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980305)76:2%3C133::aid-ajmg5%3E3.0.co;2-u. Acesso em: 28 mar. 2024.
    • APA

      Guion-Almeida, M. L., Rodini, E. S. O., Nakata, N. M. K., & Amantini, D. B. (1998). Blepharo-cheilo-dontic (BCD) syndrome: report on four new patients. American Journal of Medical Genetics, 76( 5), 133-136. doi:10.1002/(sici)1096-8628(19980305)76:2%3C133::aid-ajmg5%3E3.0.co;2-u
    • NLM

      Guion-Almeida ML, Rodini ESO, Nakata NMK, Amantini DB. Blepharo-cheilo-dontic (BCD) syndrome: report on four new patients [Internet]. American Journal of Medical Genetics. 1998 ; 76( 5): 133-136.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980305)76:2%3C133::aid-ajmg5%3E3.0.co;2-u
    • Vancouver

      Guion-Almeida ML, Rodini ESO, Nakata NMK, Amantini DB. Blepharo-cheilo-dontic (BCD) syndrome: report on four new patients [Internet]. American Journal of Medical Genetics. 1998 ; 76( 5): 133-136.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980305)76:2%3C133::aid-ajmg5%3E3.0.co;2-u
  • Source: American Journal of Medical Genetics. Unidades: FOB, HRAC

    Subjects: TRANSTORNOS DA AUDIÇÃO, SURDO

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      VITTO, Luciana Paula Maximino de et al. New autosomal recessive syndrome of progressive sensorineural hearing loss and cataracts: report on two brazilian patients. American Journal of Medical Genetics, v. 70, n. 3, p. 247-249, 1997Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19970613)70:3%3C247::aid-ajmg6%3E3.0.co;2-t. Acesso em: 28 mar. 2024.
    • APA

      Vitto, L. P. M. de, Costa Filho, O. A., Bevilacqua, M. C., Passerotti, S., & Richieri-Costa, A. (1997). New autosomal recessive syndrome of progressive sensorineural hearing loss and cataracts: report on two brazilian patients. American Journal of Medical Genetics, 70( 3), 247-249. doi:10.1002/(sici)1096-8628(19970613)70:3%3C247::aid-ajmg6%3E3.0.co;2-t
    • NLM

      Vitto LPM de, Costa Filho OA, Bevilacqua MC, Passerotti S, Richieri-Costa A. New autosomal recessive syndrome of progressive sensorineural hearing loss and cataracts: report on two brazilian patients [Internet]. American Journal of Medical Genetics. 1997 ; 70( 3): 247-249.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970613)70:3%3C247::aid-ajmg6%3E3.0.co;2-t
    • Vancouver

      Vitto LPM de, Costa Filho OA, Bevilacqua MC, Passerotti S, Richieri-Costa A. New autosomal recessive syndrome of progressive sensorineural hearing loss and cataracts: report on two brazilian patients [Internet]. American Journal of Medical Genetics. 1997 ; 70( 3): 247-249.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970613)70:3%3C247::aid-ajmg6%3E3.0.co;2-t
  • Source: American Journal of Medical Genetics. Unidades: IB, HRAC

    Subjects: SÍNDROMES OROFACIODIGITAIS, MUTAÇÃO, POLIMORFISMO

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    • ABNT

      PASSOS-BUENO, Maria Rita e SERTIÉ, Andréa Laurato e RICHIERI-COSTA, Antonio. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene?. American Journal of Medical Genetics, v. 71, n. 2, p. 243-245, 1997Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d. Acesso em: 28 mar. 2024.
    • APA

      Passos-Bueno, M. R., Sertié, A. L., & Richieri-Costa, A. (1997). Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? American Journal of Medical Genetics, 71( 2), 243-245. doi:10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d
    • NLM

      Passos-Bueno MR, Sertié AL, Richieri-Costa A. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 243-245.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d
    • Vancouver

      Passos-Bueno MR, Sertié AL, Richieri-Costa A. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 243-245.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subjects: ANORMALIDADES CRANIOFACIAIS, FISSURA LÁBIOPALATINA

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      RICHIERI-COSTA, Antonio e BRANDÃO-ALMEIDA, Iara Lêda. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected brazilian patient born to consanguineous parents. American Journal of Medical Genetics, v. 71, n. 2, p. 233-235, 1997Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C233::aid-ajmg23%3E3.0.co;2-e. Acesso em: 28 mar. 2024.
    • APA

      Richieri-Costa, A., & Brandão-Almeida, I. L. (1997). Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected brazilian patient born to consanguineous parents. American Journal of Medical Genetics, 71( 2), 233-235. doi:10.1002/(sici)1096-8628(19970808)71:2%3C233::aid-ajmg23%3E3.0.co;2-e
    • NLM

      Richieri-Costa A, Brandão-Almeida IL. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected brazilian patient born to consanguineous parents [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 233-235.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C233::aid-ajmg23%3E3.0.co;2-e
    • Vancouver

      Richieri-Costa A, Brandão-Almeida IL. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected brazilian patient born to consanguineous parents [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 233-235.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C233::aid-ajmg23%3E3.0.co;2-e
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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      GUION-ALMEIDA, Maria Leine et al. Cerebrofaciothoracic syndrome. American Journal of Medical Genetics, v. 61, n. Ja 1996, p. 152-153, 1996Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C152::aid-ajmg9%3E3.0.co;2-z. Acesso em: 28 mar. 2024.
    • APA

      Guion-Almeida, M. L., Richieri-Costa, A., Saavedra, D., & Cohen Junior, M. M. (1996). Cerebrofaciothoracic syndrome. American Journal of Medical Genetics, 61( Ja 1996), 152-153. doi:10.1002/(sici)1096-8628(19960111)61:2%3C152::aid-ajmg9%3E3.0.co;2-z
    • NLM

      Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen Junior MM. Cerebrofaciothoracic syndrome [Internet]. American Journal of Medical Genetics. 1996 ; 61( Ja 1996): 152-153.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C152::aid-ajmg9%3E3.0.co;2-z
    • Vancouver

      Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen Junior MM. Cerebrofaciothoracic syndrome [Internet]. American Journal of Medical Genetics. 1996 ; 61( Ja 1996): 152-153.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C152::aid-ajmg9%3E3.0.co;2-z
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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      TABITH JUNIOR, Alfredo e BENTO-GONÇALVES, Cristina Guedes de Azevedo. Laryngeal malformations in the Richieri-Costa and Pereira form of acrofacial dysostosis. American Journal of Medical Genetics, v. 66, n. 4, p. 399-402, 1996Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19961230)66:4%3C399::aid-ajmg3%3E3.0.co;2-g. Acesso em: 28 mar. 2024.
    • APA

      Tabith Junior, A., & Bento-Gonçalves, C. G. de A. (1996). Laryngeal malformations in the Richieri-Costa and Pereira form of acrofacial dysostosis. American Journal of Medical Genetics, 66( 4), 399-402. doi:10.1002/(sici)1096-8628(19961230)66:4%3C399::aid-ajmg3%3E3.0.co;2-g
    • NLM

      Tabith Junior A, Bento-Gonçalves CG de A. Laryngeal malformations in the Richieri-Costa and Pereira form of acrofacial dysostosis [Internet]. American Journal of Medical Genetics. 1996 ; 66( 4): 399-402.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19961230)66:4%3C399::aid-ajmg3%3E3.0.co;2-g
    • Vancouver

      Tabith Junior A, Bento-Gonçalves CG de A. Laryngeal malformations in the Richieri-Costa and Pereira form of acrofacial dysostosis [Internet]. American Journal of Medical Genetics. 1996 ; 66( 4): 399-402.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19961230)66:4%3C399::aid-ajmg3%3E3.0.co;2-g
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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      SAAVEDRA, Dolores et al. Craniofrontonasal syndrome: study of 41 patients. American Journal of Medical Genetics, v. 61, n. Ja 1996, p. 147-151, 1996Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C147::aid-ajmg8%3E3.0.co;2-u. Acesso em: 28 mar. 2024.
    • APA

      Saavedra, D., Richieri-Costa, A., Guion-Almeida, M. L., & Cohen Junior, M. M. (1996). Craniofrontonasal syndrome: study of 41 patients. American Journal of Medical Genetics, 61( Ja 1996), 147-151. doi:10.1002/(sici)1096-8628(19960111)61:2%3C147::aid-ajmg8%3E3.0.co;2-u
    • NLM

      Saavedra D, Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Craniofrontonasal syndrome: study of 41 patients [Internet]. American Journal of Medical Genetics. 1996 ; 61( Ja 1996): 147-151.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C147::aid-ajmg8%3E3.0.co;2-u
    • Vancouver

      Saavedra D, Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Craniofrontonasal syndrome: study of 41 patients [Internet]. American Journal of Medical Genetics. 1996 ; 61( Ja 1996): 147-151.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19960111)61:2%3C147::aid-ajmg8%3E3.0.co;2-u
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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      GUION-ALMEIDA, Maria Leine. Apparent malpuech syndrome: report on three Brazilian patients with additional signs. American Journal of Medical Genetics, v. 58, n. 1, p. 13-17, 1995Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320580104. Acesso em: 28 mar. 2024.
    • APA

      Guion-Almeida, M. L. (1995). Apparent malpuech syndrome: report on three Brazilian patients with additional signs. American Journal of Medical Genetics, 58( 1), 13-17. doi:10.1002/ajmg.1320580104
    • NLM

      Guion-Almeida ML. Apparent malpuech syndrome: report on three Brazilian patients with additional signs [Internet]. American Journal of Medical Genetics. 1995 ; 58( 1): 13-17.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320580104
    • Vancouver

      Guion-Almeida ML. Apparent malpuech syndrome: report on three Brazilian patients with additional signs [Internet]. American Journal of Medical Genetics. 1995 ; 58( 1): 13-17.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320580104
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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      GUION-ALMEIDA, Maria Leine e RODINI, Elaine Sbroggio de Oliveira. Michels syndrome in a Brazilian girl born to consanguineous parents. American Journal of Medical Genetics, v. 57, n. 3, p. 377-379, 1995Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320570302. Acesso em: 28 mar. 2024.
    • APA

      Guion-Almeida, M. L., & Rodini, E. S. de O. (1995). Michels syndrome in a Brazilian girl born to consanguineous parents. American Journal of Medical Genetics, 57( 3), 377-379. doi:10.1002/ajmg.1320570302
    • NLM

      Guion-Almeida ML, Rodini ES de O. Michels syndrome in a Brazilian girl born to consanguineous parents [Internet]. American Journal of Medical Genetics. 1995 ; 57( 3): 377-379.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320570302
    • Vancouver

      Guion-Almeida ML, Rodini ES de O. Michels syndrome in a Brazilian girl born to consanguineous parents [Internet]. American Journal of Medical Genetics. 1995 ; 57( 3): 377-379.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320570302
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA

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      RICHIERI-COSTA, A et al. Newly recognized autosomal recessive faciothoracoskeletal syndrome. American Journal of Medical Genetics, v. 49, n. 2, p. 224-228, 1994Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320490213. Acesso em: 28 mar. 2024.
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      Richieri-Costa, A., Guion-Almeida, M. L., Lauris, J. R. P., & Ferreira, D. M. (1994). Newly recognized autosomal recessive faciothoracoskeletal syndrome. American Journal of Medical Genetics, 49( 2), 224-228. doi:10.1002/ajmg.1320490213
    • NLM

      Richieri-Costa A, Guion-Almeida ML, Lauris JRP, Ferreira DM. Newly recognized autosomal recessive faciothoracoskeletal syndrome [Internet]. American Journal of Medical Genetics. 1994 ; 49( 2): 224-228.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320490213
    • Vancouver

      Richieri-Costa A, Guion-Almeida ML, Lauris JRP, Ferreira DM. Newly recognized autosomal recessive faciothoracoskeletal syndrome [Internet]. American Journal of Medical Genetics. 1994 ; 49( 2): 224-228.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320490213
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subjects: ANORMALIDADES MÚLTIPLAS, GENÉTICA MÉDICA

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      RICHIERI-COSTA, Antonio e GORLIN, Robert J. Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity. American Journal of Medical Genetics, v. No 1994, n. 3, p. 222-226, 1994Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320530305. Acesso em: 28 mar. 2024.
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      Richieri-Costa, A., & Gorlin, R. J. (1994). Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity. American Journal of Medical Genetics, No 1994( 3), 222-226. doi:10.1002/ajmg.1320530305
    • NLM

      Richieri-Costa A, Gorlin RJ. Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity [Internet]. American Journal of Medical Genetics. 1994 ; No 1994( 3): 222-226.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320530305
    • Vancouver

      Richieri-Costa A, Gorlin RJ. Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity [Internet]. American Journal of Medical Genetics. 1994 ; No 1994( 3): 222-226.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320530305
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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      RICHIERI-COSTA, Antonio e GUION-ALMEIDA, Maria Leine e COHEN JUNIOR, M. Michael. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics, v. 47, n. 2, p. 278-280, 1993Tradução . . Acesso em: 28 mar. 2024.
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      Richieri-Costa, A., Guion-Almeida, M. L., & Cohen Junior, M. M. (1993). Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics, 47( 2), 278-280.
    • NLM

      Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics. 1993 ; 47( 2): 278-280.[citado 2024 mar. 28 ]
    • Vancouver

      Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics. 1993 ; 47( 2): 278-280.[citado 2024 mar. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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      RICHIERI-COSTA, Antonio e PIROLO JUNIOR, L e COHEN JUNIOR, M. Michael. Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents. American Journal of Medical Genetics, v. 47, n. 2, p. 281-283, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320470228. Acesso em: 28 mar. 2024.
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      Richieri-Costa, A., Pirolo Junior, L., & Cohen Junior, M. M. (1993). Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents. American Journal of Medical Genetics, 47( 2), 281-283. doi:10.1002/ajmg.1320470228
    • NLM

      Richieri-Costa A, Pirolo Junior L, Cohen Junior MM. Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents [Internet]. American Journal of Medical Genetics. 1993 ; 47( 2): 281-283.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320470228
    • Vancouver

      Richieri-Costa A, Pirolo Junior L, Cohen Junior MM. Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents [Internet]. American Journal of Medical Genetics. 1993 ; 47( 2): 281-283.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320470228
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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      RICHIERI-COSTA, Antonio et al. Newly recognized blepharofacioskeletal syndrome. American Journal of Medical Genetics, v. 46, n. 6, p. 620-622, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460603. Acesso em: 28 mar. 2024.
    • APA

      Richieri-Costa, A., Guion-Almeida, M. L., Rodini, E. S. de O., Pereira, S. C. D., & Cohen Junior, M. M. (1993). Newly recognized blepharofacioskeletal syndrome. American Journal of Medical Genetics, 46( 6), 620-622. doi:10.1002/ajmg.1320460603
    • NLM

      Richieri-Costa A, Guion-Almeida ML, Rodini ES de O, Pereira SCD, Cohen Junior MM. Newly recognized blepharofacioskeletal syndrome [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 620-622.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320460603
    • Vancouver

      Richieri-Costa A, Guion-Almeida ML, Rodini ES de O, Pereira SCD, Cohen Junior MM. Newly recognized blepharofacioskeletal syndrome [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 620-622.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320460603
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Subjects: ANORMALIDADES CRANIOFACIAIS, FISSURA PALATINA, RETARDO MENTAL

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      NAKATA, Nancy Mizue Kokitsu e GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity. American Journal of Medical Genetics, v. 47, n. 1, p. 330-332, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320470307. Acesso em: 28 mar. 2024.
    • APA

      Nakata, N. M. K., Guion-Almeida, M. L., & Richieri-Costa, A. (1993). Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity. American Journal of Medical Genetics, 47( 1), 330-332. doi:10.1002/ajmg.1320470307
    • NLM

      Nakata NMK, Guion-Almeida ML, Richieri-Costa A. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity [Internet]. American Journal of Medical Genetics. 1993 ; 47( 1): 330-332.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320470307
    • Vancouver

      Nakata NMK, Guion-Almeida ML, Richieri-Costa A. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity [Internet]. American Journal of Medical Genetics. 1993 ; 47( 1): 330-332.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320470307
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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    • ABNT

      RICHIERI-COSTA, Antonio et al. Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance. American Journal of Medical Genetics, v. 46, n. 6, p. 659-664, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460611. Acesso em: 28 mar. 2024.
    • APA

      Richieri-Costa, A., Bortolozo, M. A., Lauris, J. R. P., Lauris, R. de C. M. C., Guion-Almeida, M. L., Marques, D., & Moreti, D. (1993). Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance. American Journal of Medical Genetics, 46( 6), 659-664. doi:10.1002/ajmg.1320460611
    • NLM

      Richieri-Costa A, Bortolozo MA, Lauris JRP, Lauris R de CMC, Guion-Almeida ML, Marques D, Moreti D. Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 659-664.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320460611
    • Vancouver

      Richieri-Costa A, Bortolozo MA, Lauris JRP, Lauris R de CMC, Guion-Almeida ML, Marques D, Moreti D. Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 659-664.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320460611
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA

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    • ABNT

      RICHIERI-COSTA, A e GUION-ALMEIDA, Maria Leine. Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause. American Journal of Medical Genetics, v. 47, n. 5, p. 702-706, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320470523. Acesso em: 28 mar. 2024.
    • APA

      Richieri-Costa, A., & Guion-Almeida, M. L. (1993). Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause. American Journal of Medical Genetics, 47( 5), 702-706. doi:10.1002/ajmg.1320470523
    • NLM

      Richieri-Costa A, Guion-Almeida ML. Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause [Internet]. American Journal of Medical Genetics. 1993 ; 47( 5): 702-706.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320470523
    • Vancouver

      Richieri-Costa A, Guion-Almeida ML. Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause [Internet]. American Journal of Medical Genetics. 1993 ; 47( 5): 702-706.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320470523
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA

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    • ABNT

      RICHIERI-COSTA, A e PEREIRA, Sonia Cristina Silveira. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients. American Journal of Medical Genetics, v. 47, n. 5, p. 707-709, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320470524. Acesso em: 28 mar. 2024.
    • APA

      Richieri-Costa, A., & Pereira, S. C. S. (1993). Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients. American Journal of Medical Genetics, 47( 5), 707-709. doi:10.1002/ajmg.1320470524
    • NLM

      Richieri-Costa A, Pereira SCS. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients [Internet]. American Journal of Medical Genetics. 1993 ; 47( 5): 707-709.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320470524
    • Vancouver

      Richieri-Costa A, Pereira SCS. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients [Internet]. American Journal of Medical Genetics. 1993 ; 47( 5): 707-709.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320470524
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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    • ABNT

      RODINI, E S O et al. Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics, v. 42, n. 3, p. 276-280, 1992Tradução . . Acesso em: 28 mar. 2024.
    • APA

      Rodini, E. S. O., Nardi, A., Guion-Almeida, M. L., & Richieri-Costa, A. (1992). Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics, 42( 3), 276-280.
    • NLM

      Rodini ESO, Nardi A, Guion-Almeida ML, Richieri-Costa A. Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics. 1992 ; 42( 3): 276-280.[citado 2024 mar. 28 ]
    • Vancouver

      Rodini ESO, Nardi A, Guion-Almeida ML, Richieri-Costa A. Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics. 1992 ; 42( 3): 276-280.[citado 2024 mar. 28 ]
  • Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: MEDICINA

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    • ABNT

      ENDE, J J van den et al. Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents. American Journal of Medical Genetics, v. 42, n. 4, p. 467-469, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320420411. Acesso em: 28 mar. 2024.
    • APA

      Ende, J. J. van den, Bever, Y. V., Rodini, E. S. O., & Richieri-Costa, A. (1992). Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents. American Journal of Medical Genetics, 42( 4), 467-469. doi:10.1002/ajmg.1320420411
    • NLM

      Ende JJ van den, Bever YV, Rodini ESO, Richieri-Costa A. Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents [Internet]. American Journal of Medical Genetics. 1992 ; 42( 4): 467-469.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320420411
    • Vancouver

      Ende JJ van den, Bever YV, Rodini ESO, Richieri-Costa A. Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents [Internet]. American Journal of Medical Genetics. 1992 ; 42( 4): 467-469.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/ajmg.1320420411

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