ReP USP - Resultado da busca

Trabalho de evento-resumo
Refined cytogenetics in patients with craniofacial abnormalities syndromes without diagnostic set (2009)
Rodrigues, Rubens Matias; Zechi-Ceide, Roseli Maria ; Sandri, Rosana Maria Cândido de Souza ; Kamiya, Tânia Yoshico; Almeida, M. L. G
Fonte: Anais. Nome do evento: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Assuntos: CITOGENÉTICA, ANORMALIDADES CRANIOFACIAIS, DIAGNÓSTICO
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ABNT
RODRIGUES, Rubens Matias et al. Refined cytogenetics in patients with craniofacial abnormalities syndromes without diagnostic set. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/871586a1-9def-478a-ae9a-cd9eede372bb/3099727.pdf. Acesso em: 22 maio 2024.
APA
Rodrigues, R. M., Zechi-Ceide, R. M., Sandri, R. M. C. de S., Kamiya, T. Y., & Almeida, M. L. G. (2009). Refined cytogenetics in patients with craniofacial abnormalities syndromes without diagnostic set. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/871586a1-9def-478a-ae9a-cd9eede372bb/3099727.pdf
NLM
Rodrigues RM, Zechi-Ceide RM, Sandri RMC de S, Kamiya TY, Almeida MLG. Refined cytogenetics in patients with craniofacial abnormalities syndromes without diagnostic set [Internet]. Anais. 2009 ;[citado 2024 maio 22 ] Available from: https://repositorio.usp.br/directbitstream/871586a1-9def-478a-ae9a-cd9eede372bb/3099727.pdf
Vancouver
Rodrigues RM, Zechi-Ceide RM, Sandri RMC de S, Kamiya TY, Almeida MLG. Refined cytogenetics in patients with craniofacial abnormalities syndromes without diagnostic set [Internet]. Anais. 2009 ;[citado 2024 maio 22 ] Available from: https://repositorio.usp.br/directbitstream/871586a1-9def-478a-ae9a-cd9eede372bb/3099727.pdf
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
Fonte: Anais. Nome do evento: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidades: FOB, HRAC, HRACF
Assuntos: 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: 22 maio 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 maio 22 ] 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 maio 22 ] Available from: https://repositorio.usp.br/directbitstream/59b585bc-903b-4e7a-8bbb-b55811629da0/3100288.pdf
Trabalho de evento-resumo
Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? (2009)
Richieri-Costa, Antonio ; Zechi-Ceide, Roseli Maria ; Guion-Almeida, Maria Leine; Ribeiro, L. A
Fonte: Anais. Nome do evento: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Assuntos: HOLOPROSENCEFALIA, IRMÃOS, MUTAÇÃO GENÉTICA
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ABNT
RICHIERI-COSTA, Antonio et al. Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/6a4a7383-730d-4fff-9892-d05bc3f24197/3100185.pdf. Acesso em: 22 maio 2024.
APA
Richieri-Costa, A., Zechi-Ceide, R. M., Guion-Almeida, M. L., & Ribeiro, L. A. (2009). Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/6a4a7383-730d-4fff-9892-d05bc3f24197/3100185.pdf
NLM
Richieri-Costa A, Zechi-Ceide RM, Guion-Almeida ML, Ribeiro LA. Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? [Internet]. Anais. 2009 ;[citado 2024 maio 22 ] Available from: https://repositorio.usp.br/directbitstream/6a4a7383-730d-4fff-9892-d05bc3f24197/3100185.pdf
Vancouver
Richieri-Costa A, Zechi-Ceide RM, Guion-Almeida ML, Ribeiro LA. Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? [Internet]. Anais. 2009 ;[citado 2024 maio 22 ] Available from: https://repositorio.usp.br/directbitstream/6a4a7383-730d-4fff-9892-d05bc3f24197/3100185.pdf
Trabalho de evento-resumo
Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations (2009)
Zechi-Ceide, Roseli Maria ; Guion-Almeida, Maria Leine; Oliveira, N. A. J; Richieri-Costa, Antonio ; Passos-Bueno, Maria Rita
Fonte: Anais. Nome do evento: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Assuntos: SÍNDROMES OROFACIODIGITAIS, FENÓTIPOS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZECHI-CEIDE, Roseli Maria et al. Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/ba673f31-b648-4c20-a481-a147f49859c6/3100222.pdf. Acesso em: 22 maio 2024.
APA
Zechi-Ceide, R. M., Guion-Almeida, M. L., Oliveira, N. A. J., Richieri-Costa, A., & Passos-Bueno, M. R. (2009). Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/ba673f31-b648-4c20-a481-a147f49859c6/3100222.pdf
NLM
Zechi-Ceide RM, Guion-Almeida ML, Oliveira NAJ, Richieri-Costa A, Passos-Bueno MR. Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations [Internet]. Anais. 2009 ;[citado 2024 maio 22 ] Available from: https://repositorio.usp.br/directbitstream/ba673f31-b648-4c20-a481-a147f49859c6/3100222.pdf
Vancouver
Zechi-Ceide RM, Guion-Almeida ML, Oliveira NAJ, Richieri-Costa A, Passos-Bueno MR. Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations [Internet]. Anais. 2009 ;[citado 2024 maio 22 ] Available from: https://repositorio.usp.br/directbitstream/ba673f31-b648-4c20-a481-a147f49859c6/3100222.pdf

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