ReP USP - Resultado da busca

Trabalho de evento-resumo periodico
'GAMA' - sarcoglycan mutations in lgmd 2c (1996)
Mcnally, E M; Bonnemann, C G; Duggan, D; Gorospe, J R M; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Zatz, Mayana ; Noguchi, S; Ozawa, E; Hoffman, E P; Kunkel, L M
Source: American Journal of Human Genetics. Conference titles: 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
MCNALLY, E M et al. 'GAMA' - sarcoglycan mutations in lgmd 2c. American Journal of Human Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 03 nov. 2024. , 1996
APA
Mcnally, E. M., Bonnemann, C. G., Duggan, D., Gorospe, J. R. M., Passos-Bueno, M. R., Vainzof, M., et al. (1996). 'GAMA' - sarcoglycan mutations in lgmd 2c. American Journal of Human Genetics. Instituto de Biociências, Universidade de São Paulo.
NLM
Mcnally EM, Bonnemann CG, Duggan D, Gorospe JRM, Passos-Bueno MR, Vainzof M, Zatz M, Noguchi S, Ozawa E, Hoffman EP, Kunkel LM. 'GAMA' - sarcoglycan mutations in lgmd 2c. American Journal of Human Genetics. 1996 ;59( 4 suppl.): a271.[citado 2024 nov. 03 ]
Vancouver
Mcnally EM, Bonnemann CG, Duggan D, Gorospe JRM, Passos-Bueno MR, Vainzof M, Zatz M, Noguchi S, Ozawa E, Hoffman EP, Kunkel LM. 'GAMA' - sarcoglycan mutations in lgmd 2c. American Journal of Human Genetics. 1996 ;59( 4 suppl.): a271.[citado 2024 nov. 03 ]
Trabalho de evento-resumo
Six autosomal recessive limb-girdle muscular dystrophies in brazil (1996)
Zatz, Mayana ; Vainzof, Mariz ; Moreira, E S; Marie, Suely Kazue Nagahashi; Bushby, K; Anderson, L; Bonnemann, C G; Mcnally, E M; Nigro, V; Kunkel, L M; Passos-Bueno, Maria Rita
Source: Abstracts. Conference titles: Limb Girdle Muscular Dystrophies Genetics Workshop. 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. Six autosomal recessive limb-girdle muscular dystrophies in brazil. 1996, Anais.. Tunis: Instituto de Biociências, Universidade de São Paulo, 1996. . Acesso em: 03 nov. 2024.
APA
Zatz, M., Vainzof, M., Moreira, E. S., Marie, S. K. N., Bushby, K., Anderson, L., et al. (1996). Six autosomal recessive limb-girdle muscular dystrophies in brazil. In Abstracts. Tunis: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Vainzof M, Moreira ES, Marie SKN, Bushby K, Anderson L, Bonnemann CG, Mcnally EM, Nigro V, Kunkel LM, Passos-Bueno MR. Six autosomal recessive limb-girdle muscular dystrophies in brazil. Abstracts. 1996 ;[citado 2024 nov. 03 ]
Vancouver
Zatz M, Vainzof M, Moreira ES, Marie SKN, Bushby K, Anderson L, Bonnemann CG, Mcnally EM, Nigro V, Kunkel LM, Passos-Bueno MR. Six autosomal recessive limb-girdle muscular dystrophies in brazil. Abstracts. 1996 ;[citado 2024 nov. 03 ]
Artigo de periodico
Mild and severe muscular dystrophy caused by a single 'GAMA'- sarcoglycan mutation (1996)
Mcnally, E M; Passos-Bueno, Maria Rita ; Bonnemann, C G; Vainzof, Mariz ; Moreira, E S; Lidov, H G W; Othmane, K B; Denton, P H; Vance, J M; Zatz, Mayana ; Kunkel, L M
Source: 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
MCNALLY, E M et al. Mild and severe muscular dystrophy caused by a single 'GAMA'- sarcoglycan mutation. American Journal of Human Genetics, v. 59, p. 1040-7, 1996Tradução . . Acesso em: 03 nov. 2024.
APA
Mcnally, E. M., Passos-Bueno, M. R., Bonnemann, C. G., Vainzof, M., Moreira, E. S., Lidov, H. G. W., et al. (1996). Mild and severe muscular dystrophy caused by a single 'GAMA'- sarcoglycan mutation. American Journal of Human Genetics, 59, 1040-7.
NLM
Mcnally EM, Passos-Bueno MR, Bonnemann CG, Vainzof M, Moreira ES, Lidov HGW, Othmane KB, Denton PH, Vance JM, Zatz M, Kunkel LM. Mild and severe muscular dystrophy caused by a single 'GAMA'- sarcoglycan mutation. American Journal of Human Genetics. 1996 ;59 1040-7.[citado 2024 nov. 03 ]
Vancouver
Mcnally EM, Passos-Bueno MR, Bonnemann CG, Vainzof M, Moreira ES, Lidov HGW, Othmane KB, Denton PH, Vance JM, Zatz M, Kunkel LM. Mild and severe muscular dystrophy caused by a single 'GAMA'- sarcoglycan mutation. American Journal of Human Genetics. 1996 ;59 1040-7.[citado 2024 nov. 03 ]
Trabalho de evento-resumo periodico
'BETA'-sarcoglycan mutations in severe limb-girdle muscular dystrophy type 2e in brazil (1996)
Bonnemann, C G; Passos-Bueno, Maria Rita ; Mcnally, E M; Vainzof, Mariz ; Moreira, E S; Noguchi, S; Ozawa, E; Zatz, Mayana ; Kunkel, L M
Source: American Journal of Human Genetics. Conference titles: 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
BONNEMANN, C G et al. 'BETA'-sarcoglycan mutations in severe limb-girdle muscular dystrophy type 2e in brazil. American Journal of Human Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 03 nov. 2024. , 1996
APA
Bonnemann, C. G., Passos-Bueno, M. R., Mcnally, E. M., Vainzof, M., Moreira, E. S., Noguchi, S., et al. (1996). 'BETA'-sarcoglycan mutations in severe limb-girdle muscular dystrophy type 2e in brazil. American Journal of Human Genetics. Instituto de Biociências, Universidade de São Paulo.
NLM
Bonnemann CG, Passos-Bueno MR, Mcnally EM, Vainzof M, Moreira ES, Noguchi S, Ozawa E, Zatz M, Kunkel LM. 'BETA'-sarcoglycan mutations in severe limb-girdle muscular dystrophy type 2e in brazil. American Journal of Human Genetics. 1996 ;59( 4 suppl.): 1434.[citado 2024 nov. 03 ]
Vancouver
Bonnemann CG, Passos-Bueno MR, Mcnally EM, Vainzof M, Moreira ES, Noguchi S, Ozawa E, Zatz M, Kunkel LM. 'BETA'-sarcoglycan mutations in severe limb-girdle muscular dystrophy type 2e in brazil. American Journal of Human Genetics. 1996 ;59( 4 suppl.): 1434.[citado 2024 nov. 03 ]
Trabalho de evento-resumo periodico
Sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies (ar-lgmd) (1996)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Moreira, E S; Bonnemann, C G; Mcnally, E M; Anderson, L V B; Nigro, V; Kunkel, L M; Zatz, Mayana
Source: American Journal of Human Genetics. Conference titles: 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
VAINZOF, Mariz et al. Sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies (ar-lgmd). American Journal of Human Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 03 nov. 2024. , 1996
APA
Vainzof, M., Passos-Bueno, M. R., Moreira, E. S., Bonnemann, C. G., Mcnally, E. M., Anderson, L. V. B., et al. (1996). Sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies (ar-lgmd). American Journal of Human Genetics. Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Passos-Bueno MR, Moreira ES, Bonnemann CG, Mcnally EM, Anderson LVB, Nigro V, Kunkel LM, Zatz M. Sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies (ar-lgmd). American Journal of Human Genetics. 1996 ;59( 4 suppl.): 1684.[citado 2024 nov. 03 ]
Vancouver
Vainzof M, Passos-Bueno MR, Moreira ES, Bonnemann CG, Mcnally EM, Anderson LVB, Nigro V, Kunkel LM, Zatz M. Sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies (ar-lgmd). American Journal of Human Genetics. 1996 ;59( 4 suppl.): 1684.[citado 2024 nov. 03 ]
Artigo de periodico
Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e) (1996)
Bonnemann, C G; Passos-Bueno, Maria Rita ; Mcnally, E M; Vainzof, Mariz ; Moreira, E S; Marie, Suely Kazue Nagahashi; Pavanello, R C M; Noguchi, S; Ozawa, E; Zatz, Mayana ; Kunkel, L M
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
BONNEMANN, C G et al. Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e). Human Molecular Genetics, v. 5 , n. 12, p. 1953-61, 1996Tradução . . Acesso em: 03 nov. 2024.
APA
Bonnemann, C. G., Passos-Bueno, M. R., Mcnally, E. M., Vainzof, M., Moreira, E. S., Marie, S. K. N., et al. (1996). Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e). Human Molecular Genetics, 5 ( 12), 1953-61.
NLM
Bonnemann CG, Passos-Bueno MR, Mcnally EM, Vainzof M, Moreira ES, Marie SKN, Pavanello RCM, Noguchi S, Ozawa E, Zatz M, Kunkel LM. Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e). Human Molecular Genetics. 1996 ;5 ( 12): 1953-61.[citado 2024 nov. 03 ]
Vancouver
Bonnemann CG, Passos-Bueno MR, Mcnally EM, Vainzof M, Moreira ES, Marie SKN, Pavanello RCM, Noguchi S, Ozawa E, Zatz M, Kunkel LM. Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e). Human Molecular Genetics. 1996 ;5 ( 12): 1953-61.[citado 2024 nov. 03 ]
Trabalho de evento-resumo periodico
The sarcoglycan complex in autosomal recessive muscular dystrophy-LGMD2C (1996)
Vainzof, Mariz ; McNally, E; Anderson, L V B; Bonnemann, C; Passos-Bueno, Maria Rita ; Kunkel, L M; Zatz, Mayana
Source: Brazilian Journal of Genetics=Revista Brasileira de Genética. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. The sarcoglycan complex in autosomal recessive muscular dystrophy-LGMD2C. Brazilian Journal of Genetics=Revista Brasileira de Genética. Rio de Janeiro: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 03 nov. 2024. , 1996
APA
Vainzof, M., McNally, E., Anderson, L. V. B., Bonnemann, C., Passos-Bueno, M. R., Kunkel, L. M., & Zatz, M. (1996). The sarcoglycan complex in autosomal recessive muscular dystrophy-LGMD2C. Brazilian Journal of Genetics=Revista Brasileira de Genética. Rio de Janeiro: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, McNally E, Anderson LVB, Bonnemann C, Passos-Bueno MR, Kunkel LM, Zatz M. The sarcoglycan complex in autosomal recessive muscular dystrophy-LGMD2C. Brazilian Journal of Genetics=Revista Brasileira de Genética. 1996 ; 19( 2): 245.[citado 2024 nov. 03 ]
Vancouver
Vainzof M, McNally E, Anderson LVB, Bonnemann C, Passos-Bueno MR, Kunkel LM, Zatz M. The sarcoglycan complex in autosomal recessive muscular dystrophy-LGMD2C. Brazilian Journal of Genetics=Revista Brasileira de Genética. 1996 ; 19( 2): 245.[citado 2024 nov. 03 ]

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