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Artigo de periodico
Richieri-Costa–Pereira syndrome: a unique acrofacial dysostosis type: an overview of the Brazilian cases (2011)
Favaro, Francine Pinheiro; Zechi-Ceide, Roseli Maria ; Alvarez, Camila Wenceslau ; Maximino, Luciana Paula ; Antunes, Luis Fernando Benedito Bergami; Richieri-Costa, Antonio ; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics Part A. Unidades: FOB, HRAC, HRACF
Subjects: SÍNDROME DE PIERRE ROBIN, FISSURA LÁBIOPALATINA, ANOMALIA CRANIOFACIAL, EXTREMIDADES (RADIOGRAFIA), MANDÍBULA (RADIOGRAFIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FAVARO, Francine Pinheiro et al. Richieri-Costa–Pereira syndrome: a unique acrofacial dysostosis type: an overview of the Brazilian cases. American Journal of Medical Genetics Part A, v. 155, n. 2, p. 322-331, 2011Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.33806. Acesso em: 12 nov. 2024.
APA
Favaro, F. P., Zechi-Ceide, R. M., Alvarez, C. W., Maximino, L. P., Antunes, L. F. B. B., Richieri-Costa, A., & Guion-Almeida, M. L. (2011). Richieri-Costa–Pereira syndrome: a unique acrofacial dysostosis type: an overview of the Brazilian cases. American Journal of Medical Genetics Part A, 155( 2), 322-331. doi:10.1002/ajmg.a.33806
NLM
Favaro FP, Zechi-Ceide RM, Alvarez CW, Maximino LP, Antunes LFBB, Richieri-Costa A, Guion-Almeida ML. Richieri-Costa–Pereira syndrome: a unique acrofacial dysostosis type: an overview of the Brazilian cases [Internet]. American Journal of Medical Genetics Part A. 2011 ; 155( 2): 322-331.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.a.33806
Vancouver
Favaro FP, Zechi-Ceide RM, Alvarez CW, Maximino LP, Antunes LFBB, Richieri-Costa A, Guion-Almeida ML. Richieri-Costa–Pereira syndrome: a unique acrofacial dysostosis type: an overview of the Brazilian cases [Internet]. American Journal of Medical Genetics Part A. 2011 ; 155( 2): 322-331.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.a.33806
Trabalho de evento-resumo
Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? (2009)
Favaro, Francine Pinheiro; Zechi-Ceide, Roseli Maria ; Maximino, Luciana Paula ; Antunes, Luis Fernando Benedito Bergami; Richieri-Costa, Antonio ; Guion-Almeida, Maria Leine
Source: Anais. Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidades: FOB, HRAC, HRACF
Subjects: SÍNDROME DE PIERRE ROBIN, ANOMALIA MAXILOMANDIBULAR, FENÓTIPOS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FAVARO, Francine Pinheiro et al. Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/59b585bc-903b-4e7a-8bbb-b55811629da0/3100288.pdf. Acesso em: 12 nov. 2024.
APA
Favaro, F. P., Zechi-Ceide, R. M., Maximino, L. P., Antunes, L. F. B. B., Richieri-Costa, A., & Guion-Almeida, M. L. (2009). Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/59b585bc-903b-4e7a-8bbb-b55811629da0/3100288.pdf
NLM
Favaro FP, Zechi-Ceide RM, Maximino LP, Antunes LFBB, Richieri-Costa A, Guion-Almeida ML. Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? [Internet]. Anais. 2009 ;[citado 2024 nov. 12 ] Available from: https://repositorio.usp.br/directbitstream/59b585bc-903b-4e7a-8bbb-b55811629da0/3100288.pdf
Vancouver
Favaro FP, Zechi-Ceide RM, Maximino LP, Antunes LFBB, Richieri-Costa A, Guion-Almeida ML. Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? [Internet]. Anais. 2009 ;[citado 2024 nov. 12 ] Available from: https://repositorio.usp.br/directbitstream/59b585bc-903b-4e7a-8bbb-b55811629da0/3100288.pdf
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
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: 12 nov. 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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e

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