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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: 09 ago. 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 ago. 09 ] 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 ago. 09 ] Available from: https://doi.org/10.1002/ajmg.a.10444
Artigo de periodico
Effects of HEMA/solvent combinations on bond strength to dentin (2003)
Carvalho, Ricardo Marins; Mendonça, J. S.; Santiago, S. L.; Silveira, R. R.; Garcia, F. C. P.; Tay, F. R.; Pashley, D. H.
Source: Journal of Dental Research. Unidade: FOB
Subjects: RESISTÊNCIA ESTRUTURAL, DENTINA, SOLVENTE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Ricardo Marins et al. Effects of HEMA/solvent combinations on bond strength to dentin. Journal of Dental Research, v. 82, n. 8, p. 597-601, 2003Tradução . . Disponível em: http://jdr.iadrjournals.org/cgi/content/full/82/8/597?maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&searchid=1073930295534_592&stored_search=&FIRSTINDEX=0&sortspec=relevance&volume=82&firstpage=59. Acesso em: 09 ago. 2024.
APA
Carvalho, R. M., Mendonça, J. S., Santiago, S. L., Silveira, R. R., Garcia, F. C. P., Tay, F. R., & Pashley, D. H. (2003). Effects of HEMA/solvent combinations on bond strength to dentin. Journal of Dental Research, 82( 8), 597-601. Recuperado de http://jdr.iadrjournals.org/cgi/content/full/82/8/597?maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&searchid=1073930295534_592&stored_search=&FIRSTINDEX=0&sortspec=relevance&volume=82&firstpage=59
NLM
Carvalho RM, Mendonça JS, Santiago SL, Silveira RR, Garcia FCP, Tay FR, Pashley DH. Effects of HEMA/solvent combinations on bond strength to dentin [Internet]. Journal of Dental Research. 2003 ; 82( 8): 597-601.[citado 2024 ago. 09 ] Available from: http://jdr.iadrjournals.org/cgi/content/full/82/8/597?maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&searchid=1073930295534_592&stored_search=&FIRSTINDEX=0&sortspec=relevance&volume=82&firstpage=59
Vancouver
Carvalho RM, Mendonça JS, Santiago SL, Silveira RR, Garcia FCP, Tay FR, Pashley DH. Effects of HEMA/solvent combinations on bond strength to dentin [Internet]. Journal of Dental Research. 2003 ; 82( 8): 597-601.[citado 2024 ago. 09 ] Available from: http://jdr.iadrjournals.org/cgi/content/full/82/8/597?maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&searchid=1073930295534_592&stored_search=&FIRSTINDEX=0&sortspec=relevance&volume=82&firstpage=59
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: 09 ago. 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 ago. 09 ] 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 ago. 09 ] 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: 09 ago. 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 ago. 09 ] 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 ago. 09 ] Available from: https://doi.org/10.1002/ajmg.a.10227
Artigo de periodico
Clinical and microbiological evaluation of the periodontal status of children with unilateral complete cleft lip and palate (2003)
Costa, Beatriz; Lima, José Eduardo de Oliveira; Gomide, Márcia Ribeiro; Rosa, Odila Pereira da Silva
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, FOB
Subjects: BACTÉRIAS AERÓBICAS, FISSURA LÁBIOPALATINA COMPLETA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Beatriz et al. Clinical and microbiological evaluation of the periodontal status of children with unilateral complete cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. No, n. 6, p. 585-589, 2003Tradução . . Acesso em: 09 ago. 2024.
APA
Costa, B., Lima, J. E. de O., Gomide, M. R., & Rosa, O. P. da S. (2003). Clinical and microbiological evaluation of the periodontal status of children with unilateral complete cleft lip and palate. The Cleft Palate-Craniofacial Journal, No( 6), 585-589.
NLM
Costa B, Lima JE de O, Gomide MR, Rosa OP da S. Clinical and microbiological evaluation of the periodontal status of children with unilateral complete cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2003 ; No( 6): 585-589.[citado 2024 ago. 09 ]
Vancouver
Costa B, Lima JE de O, Gomide MR, Rosa OP da S. Clinical and microbiological evaluation of the periodontal status of children with unilateral complete cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2003 ; No( 6): 585-589.[citado 2024 ago. 09 ]
Artigo de periodico
Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient (2003)
Guion-Almeida, Maria Leine; Lopes, Vera Lúcia Gil da Silva
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: HIPERTELORISMO, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e LOPES, Vera Lúcia Gil da Silva. Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient. Clinical Dysmorphology, v. 12, n. 4, p. 233-236, 2003Tradução . . Disponível em: https://doi.org/10.1097/00019605-200310000-00004. Acesso em: 09 ago. 2024.
APA
Guion-Almeida, M. L., & Lopes, V. L. G. da S. (2003). Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient. Clinical Dysmorphology, 12( 4), 233-236. doi:10.1097/00019605-200310000-00004
NLM
Guion-Almeida ML, Lopes VLG da S. Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient [Internet]. Clinical Dysmorphology. 2003 ; 12( 4): 233-236.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1097/00019605-200310000-00004
Vancouver
Guion-Almeida ML, Lopes VLG da S. Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient [Internet]. Clinical Dysmorphology. 2003 ; 12( 4): 233-236.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1097/00019605-200310000-00004
Artigo de periodico
Nasopharyngoscopy in Robin sequence: clinical and predictive value (2003)
Sousa, Telma Vidotto de; Marques, Ilza Lazarini; Carneiro, Araken Fernando; Bettiol, Heloisa; Freitas, José Alberto de Souza
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, FMRP, FOB
Subjects: SÍNDROME DE PIERRE ROBIN, NASOFARINGE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUSA, Telma Vidotto de et al. Nasopharyngoscopy in Robin sequence: clinical and predictive value. The Cleft Palate-Craniofacial Journal, v. No 2003, n. 6, p. 618-623, 2003Tradução . . Acesso em: 09 ago. 2024.
APA
Sousa, T. V. de, Marques, I. L., Carneiro, A. F., Bettiol, H., & Freitas, J. A. de S. (2003). Nasopharyngoscopy in Robin sequence: clinical and predictive value. The Cleft Palate-Craniofacial Journal, No 2003( 6), 618-623.
NLM
Sousa TV de, Marques IL, Carneiro AF, Bettiol H, Freitas JA de S. Nasopharyngoscopy in Robin sequence: clinical and predictive value. The Cleft Palate-Craniofacial Journal. 2003 ; No 2003( 6): 618-623.[citado 2024 ago. 09 ]
Vancouver
Sousa TV de, Marques IL, Carneiro AF, Bettiol H, Freitas JA de S. Nasopharyngoscopy in Robin sequence: clinical and predictive value. The Cleft Palate-Craniofacial Journal. 2003 ; No 2003( 6): 618-623.[citado 2024 ago. 09 ]
Artigo de periodico
Waardenburg syndrome: clinical differentiation between types I and II (2003)
Pardono, Eliete; Bever, Yolande van; Ende, Jenneke van den; Havrenne, Poti Chimetta; Iughetti, Paula; Maestrelli, Sylvia Regina Pedrosa; Costa Filho, Orozimbo Alves; Richieri-Costa, Antonio; Frota-Pessoa, Oswaldo; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidades: FOB, HRAC, IB
Assunto: ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARDONO, Eliete et al. Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, v. 117A, n. 3, p. 223-235, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10193. Acesso em: 09 ago. 2024.
APA
Pardono, E., Bever, Y. van, Ende, J. van den, Havrenne, P. C., Iughetti, P., Maestrelli, S. R. P., et al. (2003). Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, 117A( 3), 223-235. doi:10.1002/ajmg.a.10193
NLM
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Vancouver
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1002/ajmg.a.10193

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