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Filtros : "FOB" "Costa Filho, Orozimbo Alves" "American Journal of Medical Genetics" Limpar

Filtros

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: 27 abr. 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 abr. 27 ] 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 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Artigo de periodico
New autosomal recessive syndrome of progressive sensorineural hearing loss and cataracts: report on two brazilian patients (1997)
Vitto, Luciana Paula Maximino de; Costa Filho, Orozimbo Alves; Bevilacqua, Maria Cecília; Passerotti, Sergio; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidades: FOB, HRAC
Subjects: TRANSTORNOS DA AUDIÇÃO, SURDO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VITTO, Luciana Paula Maximino de et al. New autosomal recessive syndrome of progressive sensorineural hearing loss and cataracts: report on two brazilian patients. American Journal of Medical Genetics, v. 70, n. 3, p. 247-249, 1997Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19970613)70:3%3C247::aid-ajmg6%3E3.0.co;2-t. Acesso em: 27 abr. 2024.
APA
Vitto, L. P. M. de, Costa Filho, O. A., Bevilacqua, M. C., Passerotti, S., & Richieri-Costa, A. (1997). New autosomal recessive syndrome of progressive sensorineural hearing loss and cataracts: report on two brazilian patients. American Journal of Medical Genetics, 70( 3), 247-249. doi:10.1002/(sici)1096-8628(19970613)70:3%3C247::aid-ajmg6%3E3.0.co;2-t
NLM
Vitto LPM de, Costa Filho OA, Bevilacqua MC, Passerotti S, Richieri-Costa A. New autosomal recessive syndrome of progressive sensorineural hearing loss and cataracts: report on two brazilian patients [Internet]. American Journal of Medical Genetics. 1997 ; 70( 3): 247-249.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970613)70:3%3C247::aid-ajmg6%3E3.0.co;2-t
Vancouver
Vitto LPM de, Costa Filho OA, Bevilacqua MC, Passerotti S, Richieri-Costa A. New autosomal recessive syndrome of progressive sensorineural hearing loss and cataracts: report on two brazilian patients [Internet]. American Journal of Medical Genetics. 1997 ; 70( 3): 247-249.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970613)70:3%3C247::aid-ajmg6%3E3.0.co;2-t

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