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Artigo de periodico
Trauma-induced dentigerous cyst involving the anterior maxilla (2007)
Sannomiya, Eduardo Kazuo; Nogueira, Marcelo de Queiroz; Diniz, Marli de Carvalho; Pacca, Francisco Octávio Teixeira; Dalben, Gisele da Silva
Source: Journal of Dentistry. Unidade: HRAC
Subjects: CISTO MAXILOMANDIBULAR, TRAUMATISMOS DENTÁRIOS, CISTO ODONTOGÊNICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANNOMIYA, Eduardo Kazuo et al. Trauma-induced dentigerous cyst involving the anterior maxilla. Journal of Dentistry, v. 74, n. 2, p. 160-163, 2007Tradução . . Acesso em: 06 jun. 2024.
APA
Sannomiya, E. K., Nogueira, M. de Q., Diniz, M. de C., Pacca, F. O. T., & Dalben, G. da S. (2007). Trauma-induced dentigerous cyst involving the anterior maxilla. Journal of Dentistry, 74( 2), 160-163.
NLM
Sannomiya EK, Nogueira M de Q, Diniz M de C, Pacca FOT, Dalben G da S. Trauma-induced dentigerous cyst involving the anterior maxilla. Journal of Dentistry. 2007 ; 74( 2): 160-163.[citado 2024 jun. 06 ]
Vancouver
Sannomiya EK, Nogueira M de Q, Diniz M de C, Pacca FOT, Dalben G da S. Trauma-induced dentigerous cyst involving the anterior maxilla. Journal of Dentistry. 2007 ; 74( 2): 160-163.[citado 2024 jun. 06 ]
Artigo de periodico
Prevalence of dental anomalies, ectopic eruption and associated oral malformations in subjects with Treacher Collins syndrome (2006)
Dalben, Gisele da Silva; Costa, Beatriz; Gomide, Marcia Ribeiro
Source: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology. Unidade: HRAC
Subjects: ANOMALIA DENTÁRIA, ERUPÇÃO DENTÁRIA, DISOSTOSE MANDIBULOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DALBEN, Gisele da Silva e COSTA, Beatriz e GOMIDE, Marcia Ribeiro. Prevalence of dental anomalies, ectopic eruption and associated oral malformations in subjects with Treacher Collins syndrome. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology, v. 101, n. 5, p. 588-592, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tripleo.2005.07.016. Acesso em: 06 jun. 2024.
APA
Dalben, G. da S., Costa, B., & Gomide, M. R. (2006). Prevalence of dental anomalies, ectopic eruption and associated oral malformations in subjects with Treacher Collins syndrome. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology, 101( 5), 588-592. doi:10.1016/j.tripleo.2005.07.016
NLM
Dalben G da S, Costa B, Gomide MR. Prevalence of dental anomalies, ectopic eruption and associated oral malformations in subjects with Treacher Collins syndrome [Internet]. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology. 2006 ; 101( 5): 588-592.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tripleo.2005.07.016
Vancouver
Dalben G da S, Costa B, Gomide MR. Prevalence of dental anomalies, ectopic eruption and associated oral malformations in subjects with Treacher Collins syndrome [Internet]. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology. 2006 ; 101( 5): 588-592.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tripleo.2005.07.016
Artigo de periodico
Oral health status of children with Treacher Collins syndrome (2006)
Dalben, Gisele da Silva; Neves, Lucimara Teixeira das; Gomide, Márcia Ribeiro
Source: Special Care in Dentistry. Unidade: HRAC
Subjects: DISOSTOSE MANDIBULOFACIAL, ÍNDICE PERIODONTAL, PLACA BACTERIANA, ESCOVAÇÃO DENTÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DALBEN, Gisele da Silva e NEVES, Lucimara Teixeira das e GOMIDE, Márcia Ribeiro. Oral health status of children with Treacher Collins syndrome. Special Care in Dentistry, v. 26, n. 2, p. 71-75, 2006Tradução . . Disponível em: https://doi.org/10.1111/j.1754-4505.2006.tb01513.x. Acesso em: 06 jun. 2024.
APA
Dalben, G. da S., Neves, L. T. das, & Gomide, M. R. (2006). Oral health status of children with Treacher Collins syndrome. Special Care in Dentistry, 26( 2), 71-75. doi:10.1111/j.1754-4505.2006.tb01513.x
NLM
Dalben G da S, Neves LT das, Gomide MR. Oral health status of children with Treacher Collins syndrome [Internet]. Special Care in Dentistry. 2006 ; 26( 2): 71-75.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1754-4505.2006.tb01513.x
Vancouver
Dalben G da S, Neves LT das, Gomide MR. Oral health status of children with Treacher Collins syndrome [Internet]. Special Care in Dentistry. 2006 ; 26( 2): 71-75.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1754-4505.2006.tb01513.x
Artigo de periodico
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases (2005)
Richieri-Costa, Antonio; Ribeiro, Lucilene Arilho
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, HOLOPROSENCEFALIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e RIBEIRO, Lucilene Arilho. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 352-353, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30628. Acesso em: 06 jun. 2024.
APA
Richieri-Costa, A., & Ribeiro, L. A. (2005). Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases. American Journal of Medical Genetics. Part A, 136( 4), 352-353. doi:10.1002/ajmg.a.30628
NLM
Richieri-Costa A, Ribeiro LA. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 352-353.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30628
Vancouver
Richieri-Costa A, Ribeiro LA. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 352-353.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30628
Artigo de periodico
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation (2005)
Ribeiro, Lucilene Arilho; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, DESENVOLVIMENTO FÍSICO, MAXILA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho e RICHIERI-COSTA, Antonio. Single median maxillary central incisor, hypophyseal tumor, and SHH mutation. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 346-347, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30625. Acesso em: 06 jun. 2024.
APA
Ribeiro, L. A., & Richieri-Costa, A. (2005). Single median maxillary central incisor, hypophyseal tumor, and SHH mutation. American Journal of Medical Genetics. Part A, 136( 4), 346-347. doi:10.1002/ajmg.a.30625
NLM
Ribeiro LA, Richieri-Costa A. Single median maxillary central incisor, hypophyseal tumor, and SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 346-347.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30625
Vancouver
Ribeiro LA, Richieri-Costa A. Single median maxillary central incisor, hypophyseal tumor, and SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 346-347.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30625
Artigo de periodico
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation (2005)
Ribeiro, Lucilene Arilho; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho e RICHIERI-COSTA, Antonio. Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 348-349, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30626. Acesso em: 06 jun. 2024.
APA
Ribeiro, L. A., & Richieri-Costa, A. (2005). Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation. American Journal of Medical Genetics. Part A, 136( 4), 348-349. doi:10.1002/ajmg.a.30626
NLM
Ribeiro LA, Richieri-Costa A. Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 348-349.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30626
Vancouver
Ribeiro LA, Richieri-Costa A. Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 348-349.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30626
Artigo de periodico
Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures (2005)
Guerra, Dania; Sanchez, Otto; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUERRA, Dania e SANCHEZ, Otto e RICHIERI-COSTA, Antonio. Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 377-380, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30665. Acesso em: 06 jun. 2024.
APA
Guerra, D., Sanchez, O., & Richieri-Costa, A. (2005). Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures. American Journal of Medical Genetics. Part A, 136( 4), 377-380. doi:10.1002/ajmg.a.30665
NLM
Guerra D, Sanchez O, Richieri-Costa A. Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 377-380.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30665
Vancouver
Guerra D, Sanchez O, Richieri-Costa A. Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 377-380.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30665
Artigo de periodico
Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects (2005)
Ribeiro, Lucilene Arilho; Guerini, Rita de Cássia Mecca; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho e GUERINI, Rita de Cássia Mecca e RICHIERI-COSTA, Antonio. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 350-351, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30627. Acesso em: 06 jun. 2024.
APA
Ribeiro, L. A., Guerini, R. de C. M., & Richieri-Costa, A. (2005). Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects. American Journal of Medical Genetics. Part A, 136( 4), 350-351. doi:10.1002/ajmg.a.30627
NLM
Ribeiro LA, Guerini R de CM, Richieri-Costa A. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 350-351.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30627
Vancouver
Ribeiro LA, Guerini R de CM, Richieri-Costa A. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 350-351.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30627
Artigo de periodico
Prevalence of palatal and alveolar cysts in babies with cleft lip and palate (2004)
Alves, Karina Mirela Ribeiro Pinto; Peixoto, Virginia; Gomide, Márcia Ribeiro; Carrara, Cleide Felício de Carvalho; Costa, Beatriz
Source: The Cleft Palate-Craniofacial Journal. Unidade: HRAC
Subjects: PROCESSO ALVEOLAR, FISSURA LÁBIOPALATINA, BEBÊS, CISTO PERIODONTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVES, Karina Mirela Ribeiro Pinto et al. Prevalence of palatal and alveolar cysts in babies with cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. 41, n. 5, p. 490-493, 2004Tradução . . Acesso em: 06 jun. 2024.
APA
Alves, K. M. R. P., Peixoto, V., Gomide, M. R., Carrara, C. F. de C., & Costa, B. (2004). Prevalence of palatal and alveolar cysts in babies with cleft lip and palate. The Cleft Palate-Craniofacial Journal, 41( 5), 490-493.
NLM
Alves KMRP, Peixoto V, Gomide MR, Carrara CF de C, Costa B. Prevalence of palatal and alveolar cysts in babies with cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 5): 490-493.[citado 2024 jun. 06 ]
Vancouver
Alves KMRP, Peixoto V, Gomide MR, Carrara CF de C, Costa B. Prevalence of palatal and alveolar cysts in babies with cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 5): 490-493.[citado 2024 jun. 06 ]
Artigo de periodico
Chronology of deciduous teeth eruption in children with cleft lip and palate (2004)
Duque, Cristiane; Dalben, Gisele da Silva; Aranha, Andreza Maria Fábio; Carrara, Cleide Felício de Carvalho; Gomide, Márcia Ribeiro; Costa, Beatriz
Source: The Cleft Palate-Craniofacial Journal. Unidade: HRAC
Subjects: DENTE DECÍDUO, ERUPÇÃO DENTÁRIA, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DUQUE, Cristiane et al. Chronology of deciduous teeth eruption in children with cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. 41, n. 3, p. 285-289, 2004Tradução . . Acesso em: 06 jun. 2024.
APA
Duque, C., Dalben, G. da S., Aranha, A. M. F., Carrara, C. F. de C., Gomide, M. R., & Costa, B. (2004). Chronology of deciduous teeth eruption in children with cleft lip and palate. The Cleft Palate-Craniofacial Journal, 41( 3), 285-289.
NLM
Duque C, Dalben G da S, Aranha AMF, Carrara CF de C, Gomide MR, Costa B. Chronology of deciduous teeth eruption in children with cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 3): 285-289.[citado 2024 jun. 06 ]
Vancouver
Duque C, Dalben G da S, Aranha AMF, Carrara CF de C, Gomide MR, Costa B. Chronology of deciduous teeth eruption in children with cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 3): 285-289.[citado 2024 jun. 06 ]
Artigo de periodico
Osseointegrated implants in the oral rehabilitation of a patient with cleft lip and palate and ectodermal dysplasia: a case report (2004)
Rezende, Maria Lúcia Rubo de; Amado, Flávio Monteiro
Source: The International Journal of Oral & Maxillofacial Implants. Unidade: HRAC
Subjects: FISSURA LÁBIOPALATINA, IMPLANTE DENTÁRIO ENDOÓSSEO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REZENDE, Maria Lúcia Rubo de e AMADO, Flávio Monteiro. Osseointegrated implants in the oral rehabilitation of a patient with cleft lip and palate and ectodermal dysplasia: a case report. The International Journal of Oral & Maxillofacial Implants, v. No/Dec. 2004, n. 6, p. 896-900, 2004Tradução . . Acesso em: 06 jun. 2024.
APA
Rezende, M. L. R. de, & Amado, F. M. (2004). Osseointegrated implants in the oral rehabilitation of a patient with cleft lip and palate and ectodermal dysplasia: a case report. The International Journal of Oral & Maxillofacial Implants, No/Dec. 2004( 6), 896-900.
NLM
Rezende MLR de, Amado FM. Osseointegrated implants in the oral rehabilitation of a patient with cleft lip and palate and ectodermal dysplasia: a case report. The International Journal of Oral & Maxillofacial Implants. 2004 ; No/Dec. 2004( 6): 896-900.[citado 2024 jun. 06 ]
Vancouver
Rezende MLR de, Amado FM. Osseointegrated implants in the oral rehabilitation of a patient with cleft lip and palate and ectodermal dysplasia: a case report. The International Journal of Oral & Maxillofacial Implants. 2004 ; No/Dec. 2004( 6): 896-900.[citado 2024 jun. 06 ]
Artigo de periodico
Growth of children with isolated Robin sequence treated by nasopharyngeal intubation: importance of a hypercaloric diet (2004)
Marques, Ilza Lazarini; Peres, Suely Prieto de Barros Almeida; Bettiol, Heloisa; Barbieri, Marco Antonio; Andrea, Mauro; Souza, Luiz de
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, FMRP
Subjects: SÍNDROME DE PIERRE ROBIN, NUTRIÇÃO DA CRIANÇA, NUTRIÇÃO INFANTIL, NASOFARINGE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARQUES, Ilza Lazarini et al. Growth of children with isolated Robin sequence treated by nasopharyngeal intubation: importance of a hypercaloric diet. The Cleft Palate-Craniofacial Journal, v. 41, n. Ja 2004, p. 53-58, 2004Tradução . . Acesso em: 06 jun. 2024.
APA
Marques, I. L., Peres, S. P. de B. A., Bettiol, H., Barbieri, M. A., Andrea, M., & Souza, L. de. (2004). Growth of children with isolated Robin sequence treated by nasopharyngeal intubation: importance of a hypercaloric diet. The Cleft Palate-Craniofacial Journal, 41( Ja 2004), 53-58.
NLM
Marques IL, Peres SP de BA, Bettiol H, Barbieri MA, Andrea M, Souza L de. Growth of children with isolated Robin sequence treated by nasopharyngeal intubation: importance of a hypercaloric diet. The Cleft Palate-Craniofacial Journal. 2004 ; 41( Ja 2004): 53-58.[citado 2024 jun. 06 ]
Vancouver
Marques IL, Peres SP de BA, Bettiol H, Barbieri MA, Andrea M, Souza L de. Growth of children with isolated Robin sequence treated by nasopharyngeal intubation: importance of a hypercaloric diet. The Cleft Palate-Craniofacial Journal. 2004 ; 41( Ja 2004): 53-58.[citado 2024 jun. 06 ]
Artigo de periodico
Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study (2004)
Passos-Bueno, Maria Rita ; Gaspar, Dinamar A.; Kamiya, Tânia Yoshico; Tescarollo, Graziela; Rabanéa, Daniel Saraiva; Richieri-Costa, Antonio; Alonso, Nivaldo; Araújo, Belmino
Source: The Cleft Palate-Craniofacial Journal. Unidades: IB, HRAC
Subjects: GENES, FISSURA LÁBIOPALATINA, GENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal, v. 41, n. 4, p. 387-391, 2004Tradução . . Acesso em: 06 jun. 2024.
APA
Passos-Bueno, M. R., Gaspar, D. A., Kamiya, T. Y., Tescarollo, G., Rabanéa, D. S., Richieri-Costa, A., et al. (2004). Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal, 41( 4), 387-391.
NLM
Passos-Bueno MR, Gaspar DA, Kamiya TY, Tescarollo G, Rabanéa DS, Richieri-Costa A, Alonso N, Araújo B. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 4): 387-391.[citado 2024 jun. 06 ]
Vancouver
Passos-Bueno MR, Gaspar DA, Kamiya TY, Tescarollo G, Rabanéa DS, Richieri-Costa A, Alonso N, Araújo B. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 4): 387-391.[citado 2024 jun. 06 ]
Artigo de periodico
TBX22 mutations are a frequent cause of cleft palate (2004)
Marçano, Ana Carolina Braga; Doudney, K.; Braybrook, C.; Squires, R.; Patton, M. A.; Lees, M. M.; Richieri-Costa, Antonio; Lidral, Andrew C.; Murray, Jeffrey C.; Moore, G.E.; Stanier, P.
Source: Journal of Medical Genetics. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, FISSURA PALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARÇANO, Ana Carolina Braga et al. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics, v. 41, n. Ja 2004, p. 68-74, 2004Tradução . . Acesso em: 06 jun. 2024.
APA
Marçano, A. C. B., Doudney, K., Braybrook, C., Squires, R., Patton, M. A., Lees, M. M., et al. (2004). TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics, 41( Ja 2004), 68-74.
NLM
Marçano ACB, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics. 2004 ; 41( Ja 2004): 68-74.[citado 2024 jun. 06 ]
Vancouver
Marçano ACB, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics. 2004 ; 41( Ja 2004): 68-74.[citado 2024 jun. 06 ]
Artigo de periodico
Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? (2004)
Guion-Almeida, Maria Leine; Paula, Ligiane Alves Machado; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e PAULA, Ligiane Alves Machado e RICHIERI-COSTA, Antonio. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome?. American Journal of Medical Genetics, v. 129A, n. 2, p. 156-161, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30153. Acesso em: 06 jun. 2024.
APA
Guion-Almeida, M. L., Paula, L. A. M., & Richieri-Costa, A. (2004). Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? American Journal of Medical Genetics, 129A( 2), 156-161. doi:10.1002/ajmg.a.30153
NLM
Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? [Internet]. American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30153
Vancouver
Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? [Internet]. American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30153
Artigo de periodico
Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment (2004)
Fernandes, Adriano Yacubian; Palhares Neto, Aristides; Giglio, Alcir; Gabarra, Roberto Colichio; Zanini, Silvio Antonio; Portela, Luis; Plese, José Píndaro Pereira
Source: Journal of Neuroradiologie. Unidades: HRAC, FM
Subjects: ANORMALIDADES CRANIOFACIAIS, CÉREBRO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERNANDES, Adriano Yacubian et al. Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment. Journal of Neuroradiologie, v. 31, n. 2, p. 116-122, 2004Tradução . . Disponível em: https://doi.org/10.1016/s0150-9861(04)96978-7. Acesso em: 06 jun. 2024.
APA
Fernandes, A. Y., Palhares Neto, A., Giglio, A., Gabarra, R. C., Zanini, S. A., Portela, L., & Plese, J. P. P. (2004). Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment. Journal of Neuroradiologie, 31( 2), 116-122. doi:10.1016/s0150-9861(04)96978-7
NLM
Fernandes AY, Palhares Neto A, Giglio A, Gabarra RC, Zanini SA, Portela L, Plese JPP. Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment [Internet]. Journal of Neuroradiologie. 2004 ; 31( 2): 116-122.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/s0150-9861(04)96978-7
Vancouver
Fernandes AY, Palhares Neto A, Giglio A, Gabarra RC, Zanini SA, Portela L, Plese JPP. Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment [Internet]. Journal of Neuroradiologie. 2004 ; 31( 2): 116-122.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/s0150-9861(04)96978-7
Artigo de periodico
Dental anomalies of the permanent lateral incisors and prevalence of hypodontia outside the cleft area in complete unilateral cleft lip and palate (2003)
Ribeiro, Luciana Lourenço; Neves, Lucimara Teixeira das; Costa, Beatriz; Gomide, Márcia Ribeiro
Source: The Cleft Palate-Craniofacial Journal. Unidade: HRAC
Subjects: ANOMALIA DENTÁRIA, FISSURA LÁBIOPALATINA COMPLETA, HIPODONTIA, DENTE PERMANENTE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Luciana Lourenço et al. Dental anomalies of the permanent lateral incisors and prevalence of hypodontia outside the cleft area in complete unilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. 40, n. 2, p. 172-175, 2003Tradução . . Acesso em: 06 jun. 2024.
APA
Ribeiro, L. L., Neves, L. T. das, Costa, B., & Gomide, M. R. (2003). Dental anomalies of the permanent lateral incisors and prevalence of hypodontia outside the cleft area in complete unilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal, 40( 2), 172-175.
NLM
Ribeiro LL, Neves LT das, Costa B, Gomide MR. Dental anomalies of the permanent lateral incisors and prevalence of hypodontia outside the cleft area in complete unilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2003 ; 40( 2): 172-175.[citado 2024 jun. 06 ]
Vancouver
Ribeiro LL, Neves LT das, Costa B, Gomide MR. Dental anomalies of the permanent lateral incisors and prevalence of hypodontia outside the cleft area in complete unilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2003 ; 40( 2): 172-175.[citado 2024 jun. 06 ]
Artigo de periodico
Acrofrontofacionasal dysostosis: report of the third Brazilian family (2003)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: DISOSTOSE CRÂNIOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Acrofrontofacionasal dysostosis: report of the third Brazilian family. American Journal of Medical Genetics, v. 119A, n. 2, p. 238-241, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10444. Acesso em: 06 jun. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (2003). Acrofrontofacionasal dysostosis: report of the third Brazilian family. American Journal of Medical Genetics, 119A( 2), 238-241. doi:10.1002/ajmg.a.10444
NLM
Guion-Almeida ML, Richieri-Costa A. Acrofrontofacionasal dysostosis: report of the third Brazilian family [Internet]. American Journal of Medical Genetics. 2003 ; 119A( 2): 238-241.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.10444
Vancouver
Guion-Almeida ML, Richieri-Costa A. Acrofrontofacionasal dysostosis: report of the third Brazilian family [Internet]. American Journal of Medical Genetics. 2003 ; 119A( 2): 238-241.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.10444
Artigo de periodico
Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? (2003)
Lopes, Vera Lúcia Gil da Silva; Guion-Almeida, Maria Leine; Rodini, Elaine Sbroggio de Oliveira
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, FISSURA LÁBIOPALATINA, HIPOTIREOIDISMO, ANOMALIA DENTÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOPES, Vera Lúcia Gil da Silva e GUION-ALMEIDA, Maria Leine e RODINI, Elaine Sbroggio de Oliveira. Blepharocheilodontic (BCD) syndrome:: expanding the phenotype?. American Journal of Medical Genetics, v. 121A, n. 3, p. 266-270, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20223. Acesso em: 06 jun. 2024.
APA
Lopes, V. L. G. da S., Guion-Almeida, M. L., & Rodini, E. S. de O. (2003). Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? American Journal of Medical Genetics, 121A( 3), 266-270. doi:10.1002/ajmg.a.20223
NLM
Lopes VLG da S, Guion-Almeida ML, Rodini ES de O. Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? [Internet]. American Journal of Medical Genetics. 2003 ; 121A( 3): 266-270.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.20223
Vancouver
Lopes VLG da S, Guion-Almeida ML, Rodini ES de O. Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? [Internet]. American Journal of Medical Genetics. 2003 ; 121A( 3): 266-270.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.20223
Artigo de periodico
Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients (2003)
Tabith Junior, Alfredo; Gonçalves, Cristina Guedes de Azevedo Bento
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: LARINGE, MALFORMAÇÕES, VOZ (FISIOLOGIA), ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TABITH JUNIOR, Alfredo e GONÇALVES, Cristina Guedes de Azevedo Bento. Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients. American Journal of Medical Genetics, v. 122A, n. 2, p. 133-138, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10227. Acesso em: 06 jun. 2024.
APA
Tabith Junior, A., & Gonçalves, C. G. de A. B. (2003). Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients. American Journal of Medical Genetics, 122A( 2), 133-138. doi:10.1002/ajmg.a.10227
NLM
Tabith Junior A, Gonçalves CG de AB. Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients [Internet]. American Journal of Medical Genetics. 2003 ; 122A( 2): 133-138.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.10227
Vancouver
Tabith Junior A, Gonçalves CG de AB. Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients [Internet]. American Journal of Medical Genetics. 2003 ; 122A( 2): 133-138.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1002/ajmg.a.10227

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