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Artigo de periodico
Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk (1992)
Passos-Bueno, Maria Rita ; Bakker, E; Kneppers, A L J; Takata, R I; Rapaport, D; Dunnen, J T; Zatz, Mayana ; Ommen, G J B
Fonte: American Journal of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk. American Journal of Human Genetics, v. no 1992, n. 5 , p. 1150-5, 1992Tradução . . Acesso em: 06 out. 2024.
APA
Passos-Bueno, M. R., Bakker, E., Kneppers, A. L. J., Takata, R. I., Rapaport, D., Dunnen, J. T., et al. (1992). Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk. American Journal of Human Genetics, no 1992( 5 ), 1150-5.
NLM
Passos-Bueno MR, Bakker E, Kneppers ALJ, Takata RI, Rapaport D, Dunnen JT, Zatz M, Ommen GJB. Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk. American Journal of Human Genetics. 1992 ; no 1992( 5 ): 1150-5.[citado 2024 out. 06 ]
Vancouver
Passos-Bueno MR, Bakker E, Kneppers ALJ, Takata RI, Rapaport D, Dunnen JT, Zatz M, Ommen GJB. Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk. American Journal of Human Genetics. 1992 ; no 1992( 5 ): 1150-5.[citado 2024 out. 06 ]
Artigo de periodico
Pre-puberal and presymptomatic diagnosis of charcot-tooth disease type 1 (1992)
Lego, R V; Martelli, L R; Lynch, E; Su, Y; Leperca, J; Chueh, J; Hurcko, O
Fonte: American Journal of Human Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEGO, R V et al. Pre-puberal and presymptomatic diagnosis of charcot-tooth disease type 1. American Journal of Human Genetics, v. 51, n. 4 , p. a260, 1992Tradução . . Acesso em: 06 out. 2024.
APA
Lego, R. V., Martelli, L. R., Lynch, E., Su, Y., Leperca, J., Chueh, J., & Hurcko, O. (1992). Pre-puberal and presymptomatic diagnosis of charcot-tooth disease type 1. American Journal of Human Genetics, 51( 4 ), a260.
NLM
Lego RV, Martelli LR, Lynch E, Su Y, Leperca J, Chueh J, Hurcko O. Pre-puberal and presymptomatic diagnosis of charcot-tooth disease type 1. American Journal of Human Genetics. 1992 ;51( 4 ): a260.[citado 2024 out. 06 ]
Vancouver
Lego RV, Martelli LR, Lynch E, Su Y, Leperca J, Chueh J, Hurcko O. Pre-puberal and presymptomatic diagnosis of charcot-tooth disease type 1. American Journal of Human Genetics. 1992 ;51( 4 ): a260.[citado 2024 out. 06 ]
Trabalho de evento-resumo periodico
Genetic heterogeneity of the autosomal recessive form of limb-girdle muscular dystrophy (1992)
Beckmann, J S; Passos-Bueno, Maria Rita ; Hillaire, D; Richard, I; Broux, O; Fougerousse, F; Vainzof, Mariz ; Young, K; Weissenbach, J; Conneally, M; Jackson, C E; Zatz, Mayana
Fonte: American Journal of Human Genetics. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BECKMANN, J S et al. Genetic heterogeneity of the autosomal recessive form of limb-girdle muscular dystrophy. American Journal of Human Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 06 out. 2024. , 1992
APA
Beckmann, J. S., Passos-Bueno, M. R., Hillaire, D., Richard, I., Broux, O., Fougerousse, F., et al. (1992). Genetic heterogeneity of the autosomal recessive form of limb-girdle muscular dystrophy. American Journal of Human Genetics. Instituto de Biociências, Universidade de São Paulo.
NLM
Beckmann JS, Passos-Bueno MR, Hillaire D, Richard I, Broux O, Fougerousse F, Vainzof M, Young K, Weissenbach J, Conneally M, Jackson CE, Zatz M. Genetic heterogeneity of the autosomal recessive form of limb-girdle muscular dystrophy. American Journal of Human Genetics. 1992 ;51( 4 suppl.): 182.[citado 2024 out. 06 ]
Vancouver
Beckmann JS, Passos-Bueno MR, Hillaire D, Richard I, Broux O, Fougerousse F, Vainzof M, Young K, Weissenbach J, Conneally M, Jackson CE, Zatz M. Genetic heterogeneity of the autosomal recessive form of limb-girdle muscular dystrophy. American Journal of Human Genetics. 1992 ;51( 4 suppl.): 182.[citado 2024 out. 06 ]

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