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Filtros : "ANORMALIDADES CRANIOFACIAIS" "Iughetti, Paula" Removido: "Graciano, Maria Ines Gandara" Limpar

Filtros

Artigo de periodico
Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant (2006)
Pardono, Eliete; Mazzeu, Juliana Forte; Lezirovitz, Karina; Auricchio, Maria Teresa Ballester de Melo; Iughetti, Paula; Nascimento, Rafaela Maria Pessutti; Mingroni Netto, Regina Celia ; Otto, Paulo A
Source: Genetics and Molecular Biology. Unidade: IB
Subjects: FACE (DEFEITO), ANORMALIDADES CRANIOFACIAIS, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARDONO, Eliete et al. Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant. Genetics and Molecular Biology, v. 29, n. 4, p. 601-604, 2006Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572006000400003. Acesso em: 02 nov. 2024.
APA
Pardono, E., Mazzeu, J. F., Lezirovitz, K., Auricchio, M. T. B. de M., Iughetti, P., Nascimento, R. M. P., et al. (2006). Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant. Genetics and Molecular Biology, 29( 4), 601-604. doi:10.1590/s1415-47572006000400003
NLM
Pardono E, Mazzeu JF, Lezirovitz K, Auricchio MTB de M, Iughetti P, Nascimento RMP, Mingroni Netto RC, Otto PA. Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant [Internet]. Genetics and Molecular Biology. 2006 ; 29( 4): 601-604.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1590/s1415-47572006000400003
Vancouver
Pardono E, Mazzeu JF, Lezirovitz K, Auricchio MTB de M, Iughetti P, Nascimento RMP, Mingroni Netto RC, Otto PA. Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant [Internet]. Genetics and Molecular Biology. 2006 ; 29( 4): 601-604.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1590/s1415-47572006000400003
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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.1002/ajmg.a.10193

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