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Artigo de periodico
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy (1995)
Passos-Bueno, Maria Rita ; Moreira, E S; Vainzof, Mariz ; Chamberlain, J; Marie, Suely Kazue Nagahashi; Pereira, L; Akiyama, J; Roberds, S L; Campbell, K P; Zatz, Mayana
Source: Human Molecular 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. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy. Human Molecular Genetics, v. 4 , n. 7 , p. 1163-7, 1995Tradução . . Disponível em: https://doi.org/10.1093/hmg/4.7.1163. Acesso em: 29 jun. 2024.
APA
Passos-Bueno, M. R., Moreira, E. S., Vainzof, M., Chamberlain, J., Marie, S. K. N., Pereira, L., et al. (1995). Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy. Human Molecular Genetics, 4 ( 7 ), 1163-7. doi:10.1093/hmg/4.7.1163
NLM
Passos-Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SKN, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy [Internet]. Human Molecular Genetics. 1995 ;4 ( 7 ): 1163-7.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1093/hmg/4.7.1163
Vancouver
Passos-Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SKN, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy [Internet]. Human Molecular Genetics. 1995 ;4 ( 7 ): 1163-7.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1093/hmg/4.7.1163
Artigo de periodico
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy (1995)
Passos-Bueno, Maria Rita ; Moreira, E S; Vainzof, Mariz ; Chamberlain, J; Marie, Suely Kazue Nagahashi; Pereira, L; Akujama, J Y; Roberds, S; Campbell, K P; Zatz, Mayana
Source: Human Molecular Genetics. Unidade: FM
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy. Human Molecular Genetics, v. 4 , n. 7 , p. 1163-7, 1995Tradução . . Disponível em: https://doi.org/10.1093/hmg/4.7.1163. Acesso em: 29 jun. 2024.
APA
Passos-Bueno, M. R., Moreira, E. S., Vainzof, M., Chamberlain, J., Marie, S. K. N., Pereira, L., et al. (1995). Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy. Human Molecular Genetics, 4 ( 7 ), 1163-7. doi:10.1093/hmg/4.7.1163
NLM
Passos-Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SKN, Pereira L, Akujama JY, Roberds S, Campbell KP, Zatz M. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy [Internet]. Human Molecular Genetics. 1995 ;4 ( 7 ): 1163-7.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1093/hmg/4.7.1163
Vancouver
Passos-Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SKN, Pereira L, Akujama JY, Roberds S, Campbell KP, Zatz M. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy [Internet]. Human Molecular Genetics. 1995 ;4 ( 7 ): 1163-7.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1093/hmg/4.7.1163
Artigo de periodico
Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy (1994)
Zatz, Mayana ; Matsumura, K; Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Pavanello, R C M; Marie, Suely Kazue Nagahashi; Campbell, K P
Source: Journal of the Neurological Sciences. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy. Journal of the Neurological Sciences, v. 123, p. 122-8, 1994Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(94)90213-5. Acesso em: 29 jun. 2024.
APA
Zatz, M., Matsumura, K., Vainzof, M., Passos-Bueno, M. R., Pavanello, R. C. M., Marie, S. K. N., & Campbell, K. P. (1994). Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy. Journal of the Neurological Sciences, 123, 122-8. doi:10.1016/0022-510x(94)90213-5
NLM
Zatz M, Matsumura K, Vainzof M, Passos-Bueno MR, Pavanello RCM, Marie SKN, Campbell KP. Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy [Internet]. Journal of the Neurological Sciences. 1994 ;123 122-8.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1016/0022-510x(94)90213-5
Vancouver
Zatz M, Matsumura K, Vainzof M, Passos-Bueno MR, Pavanello RCM, Marie SKN, Campbell KP. Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy [Internet]. Journal of the Neurological Sciences. 1994 ;123 122-8.[citado 2024 jun. 29 ] Available from: https://doi.org/10.1016/0022-510x(94)90213-5
Artigo de periodico
Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis (1993)
Passos-Bueno, Maria Rita ; Oliveira, J. R.; Bakker, E; Anderson, R D; Marie, Suely Kazue Nagahashi; Vainzof, Mariz ; Roberds, S; Campbell, K P; Zatz, Mayana
Source: Human Molecular 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. Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics, v. 2 , n. 11, p. 1945-7, 1993Tradução . . Acesso em: 29 jun. 2024.
APA
Passos-Bueno, M. R., Oliveira, J. R., Bakker, E., Anderson, R. D., Marie, S. K. N., Vainzof, M., et al. (1993). Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics, 2 ( 11), 1945-7.
NLM
Passos-Bueno MR, Oliveira JR, Bakker E, Anderson RD, Marie SKN, Vainzof M, Roberds S, Campbell KP, Zatz M. Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics. 1993 ;2 ( 11): 1945-7.[citado 2024 jun. 29 ]
Vancouver
Passos-Bueno MR, Oliveira JR, Bakker E, Anderson RD, Marie SKN, Vainzof M, Roberds S, Campbell KP, Zatz M. Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis. Human Molecular Genetics. 1993 ;2 ( 11): 1945-7.[citado 2024 jun. 29 ]

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