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Artigo de periodico
Apert and Crouzon syndromes: cognitive development, brain abnormalities, and molecular aspects (2016)
Fernandes, Marilyse B. L.; Maximino, Luciana P.; Perosa, Gimol B.; Abramides, Dagma V. M.; Passos-Bueno, Maria Rita ; Yacubian-Fernandes, Adriano
Source: American Journal of Medical Genetics. Part A. Unidades: FOB, IB
Subjects: CRANIOSSINOSTOSE, APTIDÃO COGNITIVA, SISTEMA NERVOSO CENTRAL, BIOLOGIA MOLECULAR, DISOSTOSE CRÂNIOFACIAL
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ABNT
FERNANDES, Marilyse B. L. et al. Apert and Crouzon syndromes: cognitive development, brain abnormalities, and molecular aspects. American Journal of Medical Genetics. Part A, v. 176, n. 6, p. 1532-1537, 2016Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.37640. Acesso em: 14 nov. 2024.
APA
Fernandes, M. B. L., Maximino, L. P., Perosa, G. B., Abramides, D. V. M., Passos-Bueno, M. R., & Yacubian-Fernandes, A. (2016). Apert and Crouzon syndromes: cognitive development, brain abnormalities, and molecular aspects. American Journal of Medical Genetics. Part A, 176( 6), 1532-1537. doi:10.1002/ajmg.a.37640
NLM
Fernandes MBL, Maximino LP, Perosa GB, Abramides DVM, Passos-Bueno MR, Yacubian-Fernandes A. Apert and Crouzon syndromes: cognitive development, brain abnormalities, and molecular aspects [Internet]. American Journal of Medical Genetics. Part A. 2016 ; 176( 6): 1532-1537.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ajmg.a.37640
Vancouver
Fernandes MBL, Maximino LP, Perosa GB, Abramides DVM, Passos-Bueno MR, Yacubian-Fernandes A. Apert and Crouzon syndromes: cognitive development, brain abnormalities, and molecular aspects [Internet]. American Journal of Medical Genetics. Part A. 2016 ; 176( 6): 1532-1537.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ajmg.a.37640
Trabalho de evento-resumo
Recurrence risks in families with nonsydromic cleft lip and palate (2013)
Santos, Daniela Vera Cruz dos ; Lauris, José Roberto Pereira ; Otto, Paulo A ; Nakata, Nancy Mizue Kokitsu
Source: Anais. Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidades: FOB, IB, HRAC, HRACF
Subjects: FISSURA LÁBIOPALATINA, FAMÍLIA, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Daniela Vera Cruz dos et al. Recurrence risks in families with nonsydromic cleft lip and palate. 2013, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2013. Disponível em: https://repositorio.usp.br/directbitstream/8921a9e0-5d5b-4266-bda7-da0dfe74ed02/2512563.pdf. Acesso em: 14 nov. 2024.
APA
Santos, D. V. C. dos, Lauris, J. R. P., Otto, P. A., & Nakata, N. M. K. (2013). Recurrence risks in families with nonsydromic cleft lip and palate. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/8921a9e0-5d5b-4266-bda7-da0dfe74ed02/2512563.pdf
NLM
Santos DVC dos, Lauris JRP, Otto PA, Nakata NMK. Recurrence risks in families with nonsydromic cleft lip and palate [Internet]. Anais. 2013 ;[citado 2024 nov. 14 ] Available from: https://repositorio.usp.br/directbitstream/8921a9e0-5d5b-4266-bda7-da0dfe74ed02/2512563.pdf
Vancouver
Santos DVC dos, Lauris JRP, Otto PA, Nakata NMK. Recurrence risks in families with nonsydromic cleft lip and palate [Internet]. Anais. 2013 ;[citado 2024 nov. 14 ] Available from: https://repositorio.usp.br/directbitstream/8921a9e0-5d5b-4266-bda7-da0dfe74ed02/2512563.pdf
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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] Available from: https://doi.org/10.1002/ajmg.a.10193

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