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Trabalho de evento-resumo periodico
Sarcoglicanopatias na população brasileira (1998)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Pavanello, Rita de Cássia M; Marie, Suely Kazue Nagahashi; Oliveira, Acary B. S.; Zatz, Mayana
Source: Genetics and Molecular Biology. Conference titles: Congresso Nacional de Genética. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Sarcoglicanopatias na população brasileira. Genetics and Molecular Biology. Ribeirão Preto: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 18 nov. 2024. , 1998
APA
Vainzof, M., Passos-Bueno, M. R., Pavanello, R. de C. M., Marie, S. K. N., Oliveira, A. B. S., & Zatz, M. (1998). Sarcoglicanopatias na população brasileira. Genetics and Molecular Biology. Ribeirão Preto: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Passos-Bueno MR, Pavanello R de CM, Marie SKN, Oliveira ABS, Zatz M. Sarcoglicanopatias na população brasileira. Genetics and Molecular Biology. 1998 ; 21( 3 suppl.): O.57.[citado 2024 nov. 18 ]
Vancouver
Vainzof M, Passos-Bueno MR, Pavanello R de CM, Marie SKN, Oliveira ABS, Zatz M. Sarcoglicanopatias na população brasileira. Genetics and Molecular Biology. 1998 ; 21( 3 suppl.): O.57.[citado 2024 nov. 18 ]
Trabalho de evento-resumo periodico
Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI) (1998)
Zatz, Mayana ; Marie, Suely Kazue Nagahashi; Cerqueira, Antonia; Vainzof, Mariz ; Pavanello, Rita C M; Passos-Bueno, Maria Rita
Source: Muscle & Nerve. Conference titles: International Congress on Neuromuscular Diseases. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI). Muscle & Nerve. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 18 nov. 2024. , 1998
APA
Zatz, M., Marie, S. K. N., Cerqueira, A., Vainzof, M., Pavanello, R. C. M., & Passos-Bueno, M. R. (1998). Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI). Muscle & Nerve. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Marie SKN, Cerqueira A, Vainzof M, Pavanello RCM, Passos-Bueno MR. Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI). Muscle & Nerve. 1998 ; 1.[citado 2024 nov. 18 ]
Vancouver
Zatz M, Marie SKN, Cerqueira A, Vainzof M, Pavanello RCM, Passos-Bueno MR. Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI). Muscle & Nerve. 1998 ; 1.[citado 2024 nov. 18 ]
Trabalho de evento
Nemaline myopathy (NM) in brazilian patients (1998)
Gurgel, J E P; Reed, Umbertina Conti; Carvalho, M. S.; Marie, Suely Kazue Nagahashi; Zatz, Mayana ; Vainzof, Mariz
Conference titles: Meeting of the International Congress of Neuromuscular Diseases. Unidades: FM, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GURGEL, J E P et al. Nemaline myopathy (NM) in brazilian patients. 1998, Anais.. Adelaide: Faculdade de Medicina, Universidade de São Paulo, 1998. . Acesso em: 18 nov. 2024.
APA
Gurgel, J. E. P., Reed, U. C., Carvalho, M. S., Marie, S. K. N., Zatz, M., & Vainzof, M. (1998). Nemaline myopathy (NM) in brazilian patients. In . Adelaide: Faculdade de Medicina, Universidade de São Paulo.
NLM
Gurgel JEP, Reed UC, Carvalho MS, Marie SKN, Zatz M, Vainzof M. Nemaline myopathy (NM) in brazilian patients. 1998 ;[citado 2024 nov. 18 ]
Vancouver
Gurgel JEP, Reed UC, Carvalho MS, Marie SKN, Zatz M, Vainzof M. Nemaline myopathy (NM) in brazilian patients. 1998 ;[citado 2024 nov. 18 ]
Artigo de periodico
Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families (1998)
Iughetti, Paula; Otto, Paulo A ; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Marie, Suely Kazue Nagahashi
Source: American Journal of Medical Genetics. Unidades: IB, FM
Assunto: DOENÇAS DEGENERATIVAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
IUGHETTI, Paula et al. Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families. American Journal of Medical Genetics, v. 77, n. 3, p. 246-248, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980518)77:3%3C246::aid-ajmg11%3E3.3.co;2-t. Acesso em: 18 nov. 2024.
APA
Iughetti, P., Otto, P. A., Zatz, M., Passos-Bueno, M. R., & Marie, S. K. N. (1998). Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families. American Journal of Medical Genetics, 77( 3), 246-248. doi:10.1002/(sici)1096-8628(19980518)77:3%3C246::aid-ajmg11%3E3.3.co;2-t
NLM
Iughetti P, Otto PA, Zatz M, Passos-Bueno MR, Marie SKN. Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families [Internet]. American Journal of Medical Genetics. 1998 ; 77( 3): 246-248.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980518)77:3%3C246::aid-ajmg11%3E3.3.co;2-t
Vancouver
Iughetti P, Otto PA, Zatz M, Passos-Bueno MR, Marie SKN. Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families [Internet]. American Journal of Medical Genetics. 1998 ; 77( 3): 246-248.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980518)77:3%3C246::aid-ajmg11%3E3.3.co;2-t
Artigo de periodico
A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies (1998)
Moreira, Eloisa S.; Vainzof, Mariz ; Marie, Suely Kazue Nagahashi; Nigro, Vicenzo; Zatz, Mayana ; Passos-Bueno, Maria Rita
Source: Journal of Medical Genetics. Unidades: FM, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA, Eloisa S. et al. A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies. Journal of Medical Genetics, v. 35, p. 951-953, 1998Tradução . . Disponível em: https://doi.org/10.1136/jmg.35.11.951. Acesso em: 18 nov. 2024.
APA
Moreira, E. S., Vainzof, M., Marie, S. K. N., Nigro, V., Zatz, M., & Passos-Bueno, M. R. (1998). A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies. Journal of Medical Genetics, 35, 951-953. doi:10.1136/jmg.35.11.951
NLM
Moreira ES, Vainzof M, Marie SKN, Nigro V, Zatz M, Passos-Bueno MR. A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies [Internet]. Journal of Medical Genetics. 1998 ; 35 951-953.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1136/jmg.35.11.951
Vancouver
Moreira ES, Vainzof M, Marie SKN, Nigro V, Zatz M, Passos-Bueno MR. A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies [Internet]. Journal of Medical Genetics. 1998 ; 35 951-953.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1136/jmg.35.11.951
Trabalho de evento-resumo
The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis (1998)
Zatz, Mayana ; Marie, Suely Kazue Nagahashi; Cerqueira, Antonia Maria Pereira; Vainzof, Mariz ; Pavanello, Rita de Cássia M; Passos-Bueno, Maria Rita
Source: Conference Handbook and Speaker Papers. Conference titles: Facioscapulohumeral Muscular Dystrophy Meeting. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. 1998, Anais.. Sydney: Instituto de Biociências, Universidade de São Paulo, 1998. . Acesso em: 18 nov. 2024.
APA
Zatz, M., Marie, S. K. N., Cerqueira, A. M. P., Vainzof, M., Pavanello, R. de C. M., & Passos-Bueno, M. R. (1998). The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. In Conference Handbook and Speaker Papers. Sydney: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Marie SKN, Cerqueira AMP, Vainzof M, Pavanello R de CM, Passos-Bueno MR. The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. Conference Handbook and Speaker Papers. 1998 ;[citado 2024 nov. 18 ]
Vancouver
Zatz M, Marie SKN, Cerqueira AMP, Vainzof M, Pavanello R de CM, Passos-Bueno MR. The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. Conference Handbook and Speaker Papers. 1998 ;[citado 2024 nov. 18 ]
Trabalho de evento-resumo periodico
Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex (1998)
Vainzof, Mariz ; Moreira, Eloisa S.; Passos-Bueno, Maria Rita ; Marie, Suely Kazue Nagahashi; Zatz, Mayana
Source: Muscle & Nerve. Conference titles: International Congress on Neuromuscular Diseases. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex. Muscle & Nerve. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 18 nov. 2024. , 1998
APA
Vainzof, M., Moreira, E. S., Passos-Bueno, M. R., Marie, S. K. N., & Zatz, M. (1998). Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex. Muscle & Nerve. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Moreira ES, Passos-Bueno MR, Marie SKN, Zatz M. Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex. Muscle & Nerve. 1998 ; 1.[citado 2024 nov. 18 ]
Vancouver
Vainzof M, Moreira ES, Passos-Bueno MR, Marie SKN, Zatz M. Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex. Muscle & Nerve. 1998 ; 1.[citado 2024 nov. 18 ]

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