Menu

Filtros : "Ceide, Roseli Maria Zechi" Limpar

Filtros

Refine with date range

21 - 32 (32 records)

  • Artigo de periodico

    Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation (2007)

    Ceide, Roseli Maria Zechi; Guion-Almeida, Maria Leine; Rodini, Elaine Sbroggio de Oliveira; Oliveira, Nélio Alessandro de Jesus; Passos-Bueno, Maria Rita

    Source: Clinical Dysmorphology. Unidades: HRAC, IB

    Subjects: MUTAÇÃO GENÉTICA, RETARDO MENTAL, ANORMALIDADES CRANIOFACIAIS

    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. Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation. Clinical Dysmorphology, v. 16, n. 3, p. 163-166, 2007Tradução . . Disponível em: https://doi.org/10.1097/MCD.0b013e3280739753. Acesso em: 23 abr. 2024.

    • APA

      Ceide, R. M. Z., Guion-Almeida, M. L., Rodini, E. S. de O., Oliveira, N. A. de J., & Passos-Bueno, M. R. (2007). Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation. Clinical Dysmorphology, 16( 3), 163-166. doi:10.1097/MCD.0b013e3280739753

    • NLM

      Ceide RMZ, Guion-Almeida ML, Rodini ES de O, Oliveira NA de J, Passos-Bueno MR. Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation [Internet]. Clinical Dysmorphology. 2007 ; 16( 3): 163-166.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1097/MCD.0b013e3280739753

    • Vancouver

      Ceide RMZ, Guion-Almeida ML, Rodini ES de O, Oliveira NA de J, Passos-Bueno MR. Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation [Internet]. Clinical Dysmorphology. 2007 ; 16( 3): 163-166.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1097/MCD.0b013e3280739753

  • Artigo de periodico

    Occipital atretic cephalocele, striking facial anomalies, and large feet in three siblings of a consanguineous union (2007)

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

    Source: American Journal of Medical Genetics. Part A. Unidade: HRAC

    Subjects: ANORMALIDADES MÚLTIPLAS, ANORMALIDADES CRANIOFACIAIS, RETARDO MENTAL

    Acesso à fonteAcesso 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. Occipital atretic cephalocele, striking facial anomalies, and large feet in three siblings of a consanguineous union. American Journal of Medical Genetics. Part A, v. 143A, n. 24, p. 3295-3301, 2007Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32019. Acesso em: 23 abr. 2024.

    • APA

      Ceide, R. M. Z., Guion-Almeida, M. L., Zanchetta, S., & Richieri-Costa, A. (2007). Occipital atretic cephalocele, striking facial anomalies, and large feet in three siblings of a consanguineous union. American Journal of Medical Genetics. Part A, 143A( 24), 3295-3301. doi:10.1002/ajmg.a.32019

    • NLM

      Ceide RMZ, Guion-Almeida ML, Zanchetta S, Richieri-Costa A. Occipital atretic cephalocele, striking facial anomalies, and large feet in three siblings of a consanguineous union [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 24): 3295-3301.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/ajmg.a.32019

    • Vancouver

      Ceide RMZ, Guion-Almeida ML, Zanchetta S, Richieri-Costa A. Occipital atretic cephalocele, striking facial anomalies, and large feet in three siblings of a consanguineous union [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 24): 3295-3301.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/ajmg.a.32019

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

    • 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: 23 abr. 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 abr. 23 ] 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 abr. 23 ] Available from: https://doi.org/10.1097/01.mcd.0000220603.09661.7e

  • Artigo de periodico

    Guadalajara camptodactyly syndrome type I: report on a new case (2002)

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

    Source: Clinical Dysmorphology. Unidade: HRAC

    Assunto: ANORMALIDADES MÚLTIPLAS

    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 e GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Guadalajara camptodactyly syndrome type I: report on a new case. Clinical Dysmorphology, v. 11, n. 2, p. 129-132, 2002Tradução . . Disponível em: https://doi.org/10.1097/00019605-200204000-00011. Acesso em: 23 abr. 2024.

    • APA

      Ceide, R. M. Z., Guion-Almeida, M. L., & Richieri-Costa, A. (2002). Guadalajara camptodactyly syndrome type I: report on a new case. Clinical Dysmorphology, 11( 2), 129-132. doi:10.1097/00019605-200204000-00011

    • NLM

      Ceide RMZ, Guion-Almeida ML, Richieri-Costa A. Guadalajara camptodactyly syndrome type I: report on a new case [Internet]. Clinical Dysmorphology. 2002 ; 11( 2): 129-132.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1097/00019605-200204000-00011

    • Vancouver

      Ceide RMZ, Guion-Almeida ML, Richieri-Costa A. Guadalajara camptodactyly syndrome type I: report on a new case [Internet]. Clinical Dysmorphology. 2002 ; 11( 2): 129-132.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1097/00019605-200204000-00011

  • Artigo de periodico

    Auriculo-condylar syndrome: additional patients (2002)

    Guion-Almeida, Maria Leine; Ceide, Roseli Maria Zechi; Vendramini, Siulan; Nakata, Nancy Mizue Kokitsu

    Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: SÍNDROMES OROFACIODIGITAIS

    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 et al. Auriculo-condylar syndrome: additional patients. American Journal of Medical Genetics, v. 112, n. 2, p. 209-214, 2002Tradução . . Disponível em: https://doi.org/10.1002/ajmg.10631. Acesso em: 23 abr. 2024.

    • APA

      Guion-Almeida, M. L., Ceide, R. M. Z., Vendramini, S., & Nakata, N. M. K. (2002). Auriculo-condylar syndrome: additional patients. American Journal of Medical Genetics, 112( 2), 209-214. doi:10.1002/ajmg.10631

    • NLM

      Guion-Almeida ML, Ceide RMZ, Vendramini S, Nakata NMK. Auriculo-condylar syndrome: additional patients [Internet]. American Journal of Medical Genetics. 2002 ; 112( 2): 209-214.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/ajmg.10631

    • Vancouver

      Guion-Almeida ML, Ceide RMZ, Vendramini S, Nakata NMK. Auriculo-condylar syndrome: additional patients [Internet]. American Journal of Medical Genetics. 2002 ; 112( 2): 209-214.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/ajmg.10631

  • Artigo de periodico

    Cleft lip/palate abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome (2000)

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

    Source: Clinical Dysmorphology. Unidade: HRAC

    Assunto: GENÉTICA

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

    • ABNT

      GUION-ALMEIDA, Maria Leine e CEIDE, Roseli Maria Zechi e RICHIERI-COSTA, Antonio. Cleft lip/palate abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome. Clinical Dysmorphology, v. 9, n. 4, p. 269-272, 2000Tradução . . Acesso em: 23 abr. 2024.

    • APA

      Guion-Almeida, M. L., Ceide, R. M. Z., & Richieri-Costa, A. (2000). Cleft lip/palate abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome. Clinical Dysmorphology, 9( 4), 269-272.

    • NLM

      Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Cleft lip/palate abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome. Clinical Dysmorphology. 2000 ; 9( 4): 269-272.[citado 2024 abr. 23 ]

    • Vancouver

      Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Cleft lip/palate abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome. Clinical Dysmorphology. 2000 ; 9( 4): 269-272.[citado 2024 abr. 23 ]

  • Artigo de periodico

    A brazilian boy with aural atresia, microtia, complex heart defect, and hearing loss (2000)

    Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu; Ceide, Roseli Maria Zechi; Vendramini, Siulan; Guerini, Rita de Cássia Mecca; Salmen, Isabel Cristina Drago Marquezine; Amaral, Natalie Camillo de Oliveira

    Source: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. Unidade: HRAC

    Subjects: GENÉTICA MÉDICA, SURDEZ

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

    • ABNT

      GUION-ALMEIDA, Maria Leine et al. A brazilian boy with aural atresia, microtia, complex heart defect, and hearing loss. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, v. 3, n. Ja, p. 23-26, 2000Tradução . . Acesso em: 23 abr. 2024.

    • APA

      Guion-Almeida, M. L., Nakata, N. M. K., Ceide, R. M. Z., Vendramini, S., Guerini, R. de C. M., Salmen, I. C. D. M., & Amaral, N. C. de O. (2000). A brazilian boy with aural atresia, microtia, complex heart defect, and hearing loss. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 3( Ja), 23-26.

    • NLM

      Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S, Guerini R de CM, Salmen ICDM, Amaral NC de O. A brazilian boy with aural atresia, microtia, complex heart defect, and hearing loss. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 2000 ; 3( Ja): 23-26.[citado 2024 abr. 23 ]

    • Vancouver

      Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S, Guerini R de CM, Salmen ICDM, Amaral NC de O. A brazilian boy with aural atresia, microtia, complex heart defect, and hearing loss. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 2000 ; 3( Ja): 23-26.[citado 2024 abr. 23 ]

  • Artigo de periodico

    Brachmann-De Lange syndrome in a mother and daughter (1999)

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

    Source: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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

    • ABNT

      CEIDE, Roseli Maria Zechi e GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Brachmann-De Lange syndrome in a mother and daughter. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, v. 2, n. Ja, p. 27-32, 1999Tradução . . Acesso em: 23 abr. 2024.

    • APA

      Ceide, R. M. Z., Guion-Almeida, M. L., & Richieri-Costa, A. (1999). Brachmann-De Lange syndrome in a mother and daughter. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 2( Ja), 27-32.

    • NLM

      Ceide RMZ, Guion-Almeida ML, Richieri-Costa A. Brachmann-De Lange syndrome in a mother and daughter. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1999 ; 2( Ja): 27-32.[citado 2024 abr. 23 ]

    • Vancouver

      Ceide RMZ, Guion-Almeida ML, Richieri-Costa A. Brachmann-De Lange syndrome in a mother and daughter. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1999 ; 2( Ja): 27-32.[citado 2024 abr. 23 ]

  • Artigo de periodico

    Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition (1999)

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

    Source: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

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

    • ABNT

      GUION-ALMEIDA, Maria Leine e CEIDE, Roseli Maria Zechi e RICHIERI-COSTA, Antonio. Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, v. 2, n. 3, p. 19-22, 1999Tradução . . Acesso em: 23 abr. 2024.

    • APA

      Guion-Almeida, M. L., Ceide, R. M. Z., & Richieri-Costa, A. (1999). Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 2( 3), 19-22.

    • NLM

      Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1999 ; 2( 3): 19-22.[citado 2024 abr. 23 ]

    • Vancouver

      Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1999 ; 2( 3): 19-22.[citado 2024 abr. 23 ]

  • Artigo de periodico

    Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients (1999)

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

    Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA

    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 CEIDE, Roseli Maria Zechi e RICHIERI-COSTA, Antonio. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients. American Journal of Medical Genetics, v. No 1999, n. 1, p. 72-77, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7. Acesso em: 23 abr. 2024.

    • APA

      Guion-Almeida, M. L., Ceide, R. M. Z., & Richieri-Costa, A. (1999). Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients. American Journal of Medical Genetics, No 1999( 1), 72-77. doi:10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7

    • NLM

      Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients [Internet]. American Journal of Medical Genetics. 1999 ; No 1999( 1): 72-77.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7

    • Vancouver

      Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients [Internet]. American Journal of Medical Genetics. 1999 ; No 1999( 1): 72-77.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7

  • Artigo de periodico

    Mandibulofacial dysostosis Bauru type syndrome: a new case (1999)

    Ceide, Roseli Maria Zechi; Guion-Almeida, Maria Leine

    Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA

    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 e GUION-ALMEIDA, Maria Leine. Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics, v. 86, n. 2, p. 199-201, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g. Acesso em: 23 abr. 2024.

    • APA

      Ceide, R. M. Z., & Guion-Almeida, M. L. (1999). Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics, 86( 2), 199-201. doi:10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g

    • NLM

      Ceide RMZ, Guion-Almeida ML. Mandibulofacial dysostosis Bauru type syndrome: a new case [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 199-201.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g

    • Vancouver

      Ceide RMZ, Guion-Almeida ML. Mandibulofacial dysostosis Bauru type syndrome: a new case [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 199-201.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g

  • Artigo de periodico

    Auriculo-condylar syndrome: further evidence for a new disorder (1999)

    Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu; Ceide, Roseli Maria Zechi; Vendramini, Siulan

    Source: American Journal of Medical Genetics. Unidade: HRAC

    Assunto: GENÉTICA MÉDICA

    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 et al. Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics, v. 86, n. 2, p. 130-133, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f. Acesso em: 23 abr. 2024.

    • APA

      Guion-Almeida, M. L., Nakata, N. M. K., Ceide, R. M. Z., & Vendramini, S. (1999). Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics, 86( 2), 130-133. doi:10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f

    • NLM

      Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S. Auriculo-condylar syndrome: further evidence for a new disorder [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 130-133.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f

    • Vancouver

      Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S. Auriculo-condylar syndrome: further evidence for a new disorder [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 130-133.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f

21 - 32 (32 records)

Digital Library of Intellectual Production of Universidade de São Paulo     2012 - 2024