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Artigo de periodico
Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome (2014)
Gordon, Christopher T.; Cunniff, Christopher M.; Green, Glenn E.; Zechi-Ceide, Roseli Maria ; Johnson, Jason M.; Henderson, Alex; Petit, Florence; Nakata, Nancy Mizue Kokitsu ; Guion-Almeida, Maria Leine; Munnich, Arnold; Cunningham, Michael L.; Lyonnet, Stanislas; Amiel, Jeanne
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Subjects: DESENVOLVIMENTO MAXILOFACIAL, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GORDON, Christopher T. et al. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome. American Journal of Medical Genetics Part A, v. 164, n. 7, p. 1850-1853, 2014Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36505. Acesso em: 16 jun. 2024.
APA
Gordon, C. T., Cunniff, C. M., Green, G. E., Zechi-Ceide, R. M., Johnson, J. M., Henderson, A., et al. (2014). Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome. American Journal of Medical Genetics Part A, 164( 7), 1850-1853. doi:10.1002/ajmg.a.36505
NLM
Gordon CT, Cunniff CM, Green GE, Zechi-Ceide RM, Johnson JM, Henderson A, Petit F, Nakata NMK, Guion-Almeida ML, Munnich A, Cunningham ML, Lyonnet S, Amiel J. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome [Internet]. American Journal of Medical Genetics Part A. 2014 ; 164( 7): 1850-1853.[citado 2024 jun. 16 ] Available from: https://doi.org/10.1002/ajmg.a.36505
Vancouver
Gordon CT, Cunniff CM, Green GE, Zechi-Ceide RM, Johnson JM, Henderson A, Petit F, Nakata NMK, Guion-Almeida ML, Munnich A, Cunningham ML, Lyonnet S, Amiel J. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome [Internet]. American Journal of Medical Genetics Part A. 2014 ; 164( 7): 1850-1853.[citado 2024 jun. 16 ] Available from: https://doi.org/10.1002/ajmg.a.36505
Artigo de periodico
A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects (2014)
Favaro, Francine Pinheiro; Alvizi, Lucas ; Zechi-Ceide, Roseli Maria; Bertola, Débora Romeo; Félix, Têmis Maria ; Souza, Josiane de; Raskin, Salmo; Twigg, Stephen R. F; Weiner, Andrea M. J; Armas, Pablo; Margarit, Ezequiel; Calcaterra, Nora B; Andersen, Gregers R; McGowan, Simon J; Wilkie, Andrew O. M; Richieri-Costa, Antonio; Almeida, Maria Leine Guion de; Passos-Bueno, Maria Rita
Source: American Journal of Human Genetics. Unidades: HRAC, IB, HRACF
Subjects: ANORMALIDADES CRANIOFACIAIS, MUTAÇÃO GENÉTICA, MALFORMAÇÕES, FISSURA PALATINA, MODELOS ANIMAIS, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FAVARO, Francine Pinheiro et al. A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects. American Journal of Human Genetics, v. 94, n. Ja 2014, p. 120-128, 2014Tradução . . Acesso em: 16 jun. 2024.
APA
Favaro, F. P., Alvizi, L., Zechi-Ceide, R. M., Bertola, D. R., Félix, T. M., Souza, J. de, et al. (2014). A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects. American Journal of Human Genetics, 94( Ja 2014), 120-128.
NLM
Favaro FP, Alvizi L, Zechi-Ceide RM, Bertola DR, Félix TM, Souza J de, Raskin S, Twigg SRF, Weiner AMJ, Armas P, Margarit E, Calcaterra NB, Andersen GR, McGowan SJ, Wilkie AOM, Richieri-Costa A, Almeida MLG de, Passos-Bueno MR. A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects. American Journal of Human Genetics. 2014 ; 94( Ja 2014): 120-128.[citado 2024 jun. 16 ]
Vancouver
Favaro FP, Alvizi L, Zechi-Ceide RM, Bertola DR, Félix TM, Souza J de, Raskin S, Twigg SRF, Weiner AMJ, Armas P, Margarit E, Calcaterra NB, Andersen GR, McGowan SJ, Wilkie AOM, Richieri-Costa A, Almeida MLG de, Passos-Bueno MR. A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects. American Journal of Human Genetics. 2014 ; 94( Ja 2014): 120-128.[citado 2024 jun. 16 ]
Artigo de periodico
Prevalence of a Simonart’s band in patients with complete cleft lip and alveolus and complete cleft lip and palate (2006)
Silva Filho, Omar Gabriel da; Santamaria Junior, Milton ; Dalben, Gisele da Silva ; Semb, Gunvor
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, FOB
Subjects: FISSURA LÁBIOPALATINA, BANDA ORTODÔNTICA, PROCESSO ALVEOLAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA FILHO, Omar Gabriel da et al. Prevalence of a Simonart’s band in patients with complete cleft lip and alveolus and complete cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. 43, n. 4, p. 442-445, 2006Tradução . . Disponível em: https://doi.org/10.1597/05-0302.1. Acesso em: 16 jun. 2024.
APA
Silva Filho, O. G. da, Santamaria Junior, M., Dalben, G. da S., & Semb, G. (2006). Prevalence of a Simonart’s band in patients with complete cleft lip and alveolus and complete cleft lip and palate. The Cleft Palate-Craniofacial Journal, 43( 4), 442-445. doi:10.1597/05-0302.1
NLM
Silva Filho OG da, Santamaria Junior M, Dalben G da S, Semb G. Prevalence of a Simonart’s band in patients with complete cleft lip and alveolus and complete cleft lip and palate [Internet]. The Cleft Palate-Craniofacial Journal. 2006 ; 43( 4): 442-445.[citado 2024 jun. 16 ] Available from: https://doi.org/10.1597/05-0302.1
Vancouver
Silva Filho OG da, Santamaria Junior M, Dalben G da S, Semb G. Prevalence of a Simonart’s band in patients with complete cleft lip and alveolus and complete cleft lip and palate [Internet]. The Cleft Palate-Craniofacial Journal. 2006 ; 43( 4): 442-445.[citado 2024 jun. 16 ] Available from: https://doi.org/10.1597/05-0302.1

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