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Trabalho de evento-resumo
Use of polymerase chain reaction (pcr) for diagnosis of duchenne muscular dystrophy (dmd) (1991)
Passos-Bueno, Maria Rita ; Rapaport, D; Takata, R I; Zatz, Mayana
Source: Resumos. Conference titles: Reuniao Anual da Sociedade Brasileira de Bioquimica e Biologia Molecular. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
PASSOS-BUENO, Maria Rita et al. Use of polymerase chain reaction (pcr) for diagnosis of duchenne muscular dystrophy (dmd). 1991, Anais.. Belo Horizonte: Universidade Federal de Minas Gerais, 1991. . Acesso em: 14 ago. 2024.
APA
Passos-Bueno, M. R., Rapaport, D., Takata, R. I., & Zatz, M. (1991). Use of polymerase chain reaction (pcr) for diagnosis of duchenne muscular dystrophy (dmd). In Resumos. Belo Horizonte: Universidade Federal de Minas Gerais.
NLM
Passos-Bueno MR, Rapaport D, Takata RI, Zatz M. Use of polymerase chain reaction (pcr) for diagnosis of duchenne muscular dystrophy (dmd). Resumos. 1991 ;[citado 2024 ago. 14 ]
Vancouver
Passos-Bueno MR, Rapaport D, Takata RI, Zatz M. Use of polymerase chain reaction (pcr) for diagnosis of duchenne muscular dystrophy (dmd). Resumos. 1991 ;[citado 2024 ago. 14 ]
Artigo de periodico
Serum creatine-kinase (ck) and pyruvate-kinase (pk) activities in duchenne (dmd) as compared with becker (bmd)muscular distrophy (1991)
Zatz, Mayana ; Rapaport, D; Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Bortolini, E R; Pavanello, R C M; Peres, C A
Source: Journal of Neurological Sciences. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
ZATZ, Mayana et al. Serum creatine-kinase (ck) and pyruvate-kinase (pk) activities in duchenne (dmd) as compared with becker (bmd)muscular distrophy. Journal of Neurological Sciences, v. 102, p. 190-6, 1991Tradução . . Acesso em: 14 ago. 2024.
APA
Zatz, M., Rapaport, D., Vainzof, M., Passos-Bueno, M. R., Bortolini, E. R., Pavanello, R. C. M., & Peres, C. A. (1991). Serum creatine-kinase (ck) and pyruvate-kinase (pk) activities in duchenne (dmd) as compared with becker (bmd)muscular distrophy. Journal of Neurological Sciences, 102, 190-6.
NLM
Zatz M, Rapaport D, Vainzof M, Passos-Bueno MR, Bortolini ER, Pavanello RCM, Peres CA. Serum creatine-kinase (ck) and pyruvate-kinase (pk) activities in duchenne (dmd) as compared with becker (bmd)muscular distrophy. Journal of Neurological Sciences. 1991 ;102 190-6.[citado 2024 ago. 14 ]
Vancouver
Zatz M, Rapaport D, Vainzof M, Passos-Bueno MR, Bortolini ER, Pavanello RCM, Peres CA. Serum creatine-kinase (ck) and pyruvate-kinase (pk) activities in duchenne (dmd) as compared with becker (bmd)muscular distrophy. Journal of Neurological Sciences. 1991 ;102 190-6.[citado 2024 ago. 14 ]
Artigo de periodico
Estimate of the intrafamilial correlation for serum creatine kinase (ck) and pyruvate kinase (pk) in females at risk for duchenne (dmd) and becker (dmb) muscular dystrophies (1991)
Rabbi-Bortolini, E; Colletto, G M D D; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Rapaport, D; Zatz, Mayana
Source: Human Heredity. Unidades: ICB, IB
Assunto: GENÉTICA MÉDICA
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ABNT
RABBI-BORTOLINI, E et al. Estimate of the intrafamilial correlation for serum creatine kinase (ck) and pyruvate kinase (pk) in females at risk for duchenne (dmd) and becker (dmb) muscular dystrophies. Human Heredity, v. no/dec. 1991, n. 6 , p. 370-8, 1991Tradução . . Acesso em: 14 ago. 2024.
APA
Rabbi-Bortolini, E., Colletto, G. M. D. D., Passos-Bueno, M. R., Vainzof, M., Rapaport, D., & Zatz, M. (1991). Estimate of the intrafamilial correlation for serum creatine kinase (ck) and pyruvate kinase (pk) in females at risk for duchenne (dmd) and becker (dmb) muscular dystrophies. Human Heredity, no/dec. 1991( 6 ), 370-8.
NLM
Rabbi-Bortolini E, Colletto GMDD, Passos-Bueno MR, Vainzof M, Rapaport D, Zatz M. Estimate of the intrafamilial correlation for serum creatine kinase (ck) and pyruvate kinase (pk) in females at risk for duchenne (dmd) and becker (dmb) muscular dystrophies. Human Heredity. 1991 ; no/dec. 1991( 6 ): 370-8.[citado 2024 ago. 14 ]
Vancouver
Rabbi-Bortolini E, Colletto GMDD, Passos-Bueno MR, Vainzof M, Rapaport D, Zatz M. Estimate of the intrafamilial correlation for serum creatine kinase (ck) and pyruvate kinase (pk) in females at risk for duchenne (dmd) and becker (dmb) muscular dystrophies. Human Heredity. 1991 ; no/dec. 1991( 6 ): 370-8.[citado 2024 ago. 14 ]
Artigo de periodico-carta/editorial
Reprodutive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimates [Carta ao editor] (1991)
Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Journal of Medical Genetics. Unidade: IB
Assunto: DISTROFIA MUSCULAR
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ABNT
PASSOS-BUENO, Maria Rita e ZATZ, Mayana. Reprodutive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimates [Carta ao editor]. Journal of Medical Genetics. London: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 14 ago. 2024. , 1991
APA
Passos-Bueno, M. R., & Zatz, M. (1991). Reprodutive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimates [Carta ao editor]. Journal of Medical Genetics. London: Instituto de Biociências, Universidade de São Paulo.
NLM
Passos-Bueno MR, Zatz M. Reprodutive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimates [Carta ao editor]. Journal of Medical Genetics. 1991 ; 28( 4): 286-287.[citado 2024 ago. 14 ]
Vancouver
Passos-Bueno MR, Zatz M. Reprodutive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimates [Carta ao editor]. Journal of Medical Genetics. 1991 ; 28( 4): 286-287.[citado 2024 ago. 14 ]
Artigo de periodico
Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in duchenne muscular dystrophy (1991)
Rapaport, D; Passos-Bueno, Maria Rita ; Brandao, L; Love, D; Vainzof, Mariz ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
RAPAPORT, D et al. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in duchenne muscular dystrophy. American Journal of Medical Genetics, v. 39, n. ju 1991, p. 437-41, 1991Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320390414. Acesso em: 14 ago. 2024.
APA
Rapaport, D., Passos-Bueno, M. R., Brandao, L., Love, D., Vainzof, M., & Zatz, M. (1991). Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in duchenne muscular dystrophy. American Journal of Medical Genetics, 39( ju 1991), 437-41. doi:10.1002/ajmg.1320390414
NLM
Rapaport D, Passos-Bueno MR, Brandao L, Love D, Vainzof M, Zatz M. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1991 ;39( ju 1991): 437-41.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/ajmg.1320390414
Vancouver
Rapaport D, Passos-Bueno MR, Brandao L, Love D, Vainzof M, Zatz M. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1991 ;39( ju 1991): 437-41.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/ajmg.1320390414
Artigo de periodico
Familial occurrence of duchenne dystrophy through paternal lines in four families (1991)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Rapaport, D; Vainzof, Mariz
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
ZATZ, Mayana et al. Familial occurrence of duchenne dystrophy through paternal lines in four families. American Journal of Medical Genetics, v. 38, n. ja 1991, p. 80-4, 1991Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320380118. Acesso em: 14 ago. 2024.
APA
Zatz, M., Passos-Bueno, M. R., Rapaport, D., & Vainzof, M. (1991). Familial occurrence of duchenne dystrophy through paternal lines in four families. American Journal of Medical Genetics, 38( ja 1991), 80-4. doi:10.1002/ajmg.1320380118
NLM
Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M. Familial occurrence of duchenne dystrophy through paternal lines in four families [Internet]. American Journal of Medical Genetics. 1991 ;38( ja 1991): 80-4.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/ajmg.1320380118
Vancouver
Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M. Familial occurrence of duchenne dystrophy through paternal lines in four families [Internet]. American Journal of Medical Genetics. 1991 ;38( ja 1991): 80-4.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/ajmg.1320380118
Artigo de periodico
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (lgmd) and 6q probes flanking the dystrophin-related sequence (1991)
Passos-Bueno, Maria Rita ; Terwilliger, J; Ott, J; Vainzof, Mariz ; Love, D R; Davies, K E; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
PASSOS-BUENO, Maria Rita et al. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (lgmd) and 6q probes flanking the dystrophin-related sequence. American Journal of Medical Genetics, v. 38, n. ja 1991, p. 140-6, 1991Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320380130. Acesso em: 14 ago. 2024.
APA
Passos-Bueno, M. R., Terwilliger, J., Ott, J., Vainzof, M., Love, D. R., Davies, K. E., & Zatz, M. (1991). Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (lgmd) and 6q probes flanking the dystrophin-related sequence. American Journal of Medical Genetics, 38( ja 1991), 140-6. doi:10.1002/ajmg.1320380130
NLM
Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (lgmd) and 6q probes flanking the dystrophin-related sequence [Internet]. American Journal of Medical Genetics. 1991 ;38( ja 1991): 140-6.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/ajmg.1320380130
Vancouver
Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (lgmd) and 6q probes flanking the dystrophin-related sequence [Internet]. American Journal of Medical Genetics. 1991 ;38( ja 1991): 140-6.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/ajmg.1320380130
Artigo de periodico
Estimates of genetic and environmental components of serum isocitrate dehydrogenase (icdh) in normal twins (1991)
Rapaport, D; Colletto, G M D D; Vainzof, Mariz ; Zatz, Mayana
Source: Acta Geneticae Medicae et Gemellologiae. Unidades: ICB, IB
Assunto: GENÉTICA MÉDICA
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ABNT
RAPAPORT, D et al. Estimates of genetic and environmental components of serum isocitrate dehydrogenase (icdh) in normal twins. Acta Geneticae Medicae et Gemellologiae, v. 40, p. 77-82, 1991Tradução . . Acesso em: 14 ago. 2024.
APA
Rapaport, D., Colletto, G. M. D. D., Vainzof, M., & Zatz, M. (1991). Estimates of genetic and environmental components of serum isocitrate dehydrogenase (icdh) in normal twins. Acta Geneticae Medicae et Gemellologiae, 40, 77-82.
NLM
Rapaport D, Colletto GMDD, Vainzof M, Zatz M. Estimates of genetic and environmental components of serum isocitrate dehydrogenase (icdh) in normal twins. Acta Geneticae Medicae et Gemellologiae. 1991 ;40 77-82.[citado 2024 ago. 14 ]
Vancouver
Rapaport D, Colletto GMDD, Vainzof M, Zatz M. Estimates of genetic and environmental components of serum isocitrate dehydrogenase (icdh) in normal twins. Acta Geneticae Medicae et Gemellologiae. 1991 ;40 77-82.[citado 2024 ago. 14 ]
Artigo de periodico
Genetic risk estimates for duchenne dystrophy ( dmd )in the absence of dna deletions in the central region of the dystrophin gene (1991)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Rapaport, D
Source: Revista Brasileira de Genetica = Brazilian Journal of Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
ZATZ, Mayana e PASSOS-BUENO, Maria Rita e RAPAPORT, D. Genetic risk estimates for duchenne dystrophy ( dmd )in the absence of dna deletions in the central region of the dystrophin gene. Revista Brasileira de Genetica = Brazilian Journal of Genetics, v. 14, n. 3 , p. 827-33, 1991Tradução . . Acesso em: 14 ago. 2024.
APA
Zatz, M., Passos-Bueno, M. R., & Rapaport, D. (1991). Genetic risk estimates for duchenne dystrophy ( dmd )in the absence of dna deletions in the central region of the dystrophin gene. Revista Brasileira de Genetica = Brazilian Journal of Genetics, 14( 3 ), 827-33.
NLM
Zatz M, Passos-Bueno MR, Rapaport D. Genetic risk estimates for duchenne dystrophy ( dmd )in the absence of dna deletions in the central region of the dystrophin gene. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1991 ;14( 3 ): 827-33.[citado 2024 ago. 14 ]
Vancouver
Zatz M, Passos-Bueno MR, Rapaport D. Genetic risk estimates for duchenne dystrophy ( dmd )in the absence of dna deletions in the central region of the dystrophin gene. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1991 ;14( 3 ): 827-33.[citado 2024 ago. 14 ]
Trabalho de evento-resumo periodico
Association of schizophrenia and becker muscular dystrophy (bmd): a susceptibility locus for schizophrenia in xp21 or an effect of the dystrophin gene in the brain? (1991)
Zatz, Mayana ; Melo, M S; Vallada, H P; Passos-Bueno, Maria Rita ; Vieira Filho, A. H. G.; Vainzof, Mariz ; Rapaport, D; Gentil Filho, Valentim
Source: Psychiatric Genetics. Conference titles: World Congress on Psychiatric Genetics. Unidades: FM, IB
Assunto: PSIQUIATRIA
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ABNT
ZATZ, Mayana et al. Association of schizophrenia and becker muscular dystrophy (bmd): a susceptibility locus for schizophrenia in xp21 or an effect of the dystrophin gene in the brain?. Psychiatric Genetics. [S.l.]: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 14 ago. 2024. , 1991
APA
Zatz, M., Melo, M. S., Vallada, H. P., Passos-Bueno, M. R., Vieira Filho, A. H. G., Vainzof, M., et al. (1991). Association of schizophrenia and becker muscular dystrophy (bmd): a susceptibility locus for schizophrenia in xp21 or an effect of the dystrophin gene in the brain? Psychiatric Genetics. Faculdade de Medicina, Universidade de São Paulo.
NLM
Zatz M, Melo MS, Vallada HP, Passos-Bueno MR, Vieira Filho AHG, Vainzof M, Rapaport D, Gentil Filho V. Association of schizophrenia and becker muscular dystrophy (bmd): a susceptibility locus for schizophrenia in xp21 or an effect of the dystrophin gene in the brain? Psychiatric Genetics. 1991 ;2 ( 1 ): 101-2.[citado 2024 ago. 14 ]
Vancouver
Zatz M, Melo MS, Vallada HP, Passos-Bueno MR, Vieira Filho AHG, Vainzof M, Rapaport D, Gentil Filho V. Association of schizophrenia and becker muscular dystrophy (bmd): a susceptibility locus for schizophrenia in xp21 or an effect of the dystrophin gene in the brain? Psychiatric Genetics. 1991 ;2 ( 1 ): 101-2.[citado 2024 ago. 14 ]
Trabalho de evento-resumo periodico
Retrospective study on the impact of diagnosis and genetic counseling in neuromuscular diseases (1991)
Eggers, S.; Zatz, Mayana ; Pavanello, R C M
Source: American Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
EGGERS, S. e ZATZ, Mayana e PAVANELLO, R C M. Retrospective study on the impact of diagnosis and genetic counseling in neuromuscular diseases. American Journal of Human Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 14 ago. 2024. , 1991
APA
Eggers, S., Zatz, M., & Pavanello, R. C. M. (1991). Retrospective study on the impact of diagnosis and genetic counseling in neuromuscular diseases. American Journal of Human Genetics. Instituto de Biociências, Universidade de São Paulo.
NLM
Eggers S, Zatz M, Pavanello RCM. Retrospective study on the impact of diagnosis and genetic counseling in neuromuscular diseases. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 311.[citado 2024 ago. 14 ]
Vancouver
Eggers S, Zatz M, Pavanello RCM. Retrospective study on the impact of diagnosis and genetic counseling in neuromuscular diseases. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 311.[citado 2024 ago. 14 ]
Artigo de periodico
Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein (1991)
Vainzof, Mariz ; Zubrzycka-Gaarn, E E; Rapaport, D; Passos-Bueno, Maria Rita ; Pavanello, R C M; Pavanello Filho, I; Zatz, Mayana
Source: Journal of the Neurological Sciences. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
VAINZOF, Mariz et al. Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein. Journal of the Neurological Sciences, v. 101, p. 141-7, 1991Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(91)90038-9. Acesso em: 14 ago. 2024.
APA
Vainzof, M., Zubrzycka-Gaarn, E. E., Rapaport, D., Passos-Bueno, M. R., Pavanello, R. C. M., Pavanello Filho, I., & Zatz, M. (1991). Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein. Journal of the Neurological Sciences, 101, 141-7. doi:10.1016/0022-510x(91)90038-9
NLM
Vainzof M, Zubrzycka-Gaarn EE, Rapaport D, Passos-Bueno MR, Pavanello RCM, Pavanello Filho I, Zatz M. Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein [Internet]. Journal of the Neurological Sciences. 1991 ;101 141-7.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/0022-510x(91)90038-9
Vancouver
Vainzof M, Zubrzycka-Gaarn EE, Rapaport D, Passos-Bueno MR, Pavanello RCM, Pavanello Filho I, Zatz M. Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein [Internet]. Journal of the Neurological Sciences. 1991 ;101 141-7.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/0022-510x(91)90038-9
Artigo de periodico
Short stature in duchenne muscular dystrophy (1991)
Rapaport, D; Colletto, G M D D; Vainzof, Mariz ; Duaik, M C D A; Zatz, Mayana
Source: Growth Regulation. Unidades: HU, ICB, IB
Assunto: GENÉTICA MÉDICA
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ABNT
RAPAPORT, D et al. Short stature in duchenne muscular dystrophy. Growth Regulation, v. 1 , n. 1 , p. 11-5, 1991Tradução . . Acesso em: 14 ago. 2024.
APA
Rapaport, D., Colletto, G. M. D. D., Vainzof, M., Duaik, M. C. D. A., & Zatz, M. (1991). Short stature in duchenne muscular dystrophy. Growth Regulation, 1 ( 1 ), 11-5.
NLM
Rapaport D, Colletto GMDD, Vainzof M, Duaik MCDA, Zatz M. Short stature in duchenne muscular dystrophy. Growth Regulation. 1991 ;1 ( 1 ): 11-5.[citado 2024 ago. 14 ]
Vancouver
Rapaport D, Colletto GMDD, Vainzof M, Duaik MCDA, Zatz M. Short stature in duchenne muscular dystrophy. Growth Regulation. 1991 ;1 ( 1 ): 11-5.[citado 2024 ago. 14 ]
Trabalho de evento-resumo periodico
Association of schizophrenia and becker dystrophy ( bmd ): a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain (1991)
Zatz, Mayana ; Melo, M S; Passos-Bueno, Maria Rita ; Valada Filho, H; Vieira Filho, A. H. G.; Vainzof, Mariz ; Rapaport, D; Gentil Filho, Valentim
Source: American Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidades: FM, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Association of schizophrenia and becker dystrophy ( bmd ): a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain. American Journal of Human Genetics. [S.l.]: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 14 ago. 2024. , 1991
APA
Zatz, M., Melo, M. S., Passos-Bueno, M. R., Valada Filho, H., Vieira Filho, A. H. G., Vainzof, M., et al. (1991). Association of schizophrenia and becker dystrophy ( bmd ): a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain. American Journal of Human Genetics. Faculdade de Medicina, Universidade de São Paulo.
NLM
Zatz M, Melo MS, Passos-Bueno MR, Valada Filho H, Vieira Filho AHG, Vainzof M, Rapaport D, Gentil Filho V. Association of schizophrenia and becker dystrophy ( bmd ): a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 364.[citado 2024 ago. 14 ]
Vancouver
Zatz M, Melo MS, Passos-Bueno MR, Valada Filho H, Vieira Filho AHG, Vainzof M, Rapaport D, Gentil Filho V. Association of schizophrenia and becker dystrophy ( bmd ): a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 364.[citado 2024 ago. 14 ]
Artigo de periodico
Screening of male patients with autosomal recessive duchenne dystrophy through dystrophin and dna studies (1991)
Vainzof, Mariz ; Pavanello, R C M; Pavanello Filho, I; Rapaport, D; Passos-Bueno, Maria Rita ; Zubrzycka-Gaarn, E E; Bulman, D E; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
VAINZOF, Mariz et al. Screening of male patients with autosomal recessive duchenne dystrophy through dystrophin and dna studies. American Journal of Medical Genetics, v. 39, p. 38-41, 1991Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320390110. Acesso em: 14 ago. 2024.
APA
Vainzof, M., Pavanello, R. C. M., Pavanello Filho, I., Rapaport, D., Passos-Bueno, M. R., Zubrzycka-Gaarn, E. E., et al. (1991). Screening of male patients with autosomal recessive duchenne dystrophy through dystrophin and dna studies. American Journal of Medical Genetics, 39, 38-41. doi:10.1002/ajmg.1320390110
NLM
Vainzof M, Pavanello RCM, Pavanello Filho I, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Bulman DE, Zatz M. Screening of male patients with autosomal recessive duchenne dystrophy through dystrophin and dna studies [Internet]. American Journal of Medical Genetics. 1991 ;39 38-41.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/ajmg.1320390110
Vancouver
Vainzof M, Pavanello RCM, Pavanello Filho I, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Bulman DE, Zatz M. Screening of male patients with autosomal recessive duchenne dystrophy through dystrophin and dna studies [Internet]. American Journal of Medical Genetics. 1991 ;39 38-41.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/ajmg.1320390110
Artigo de periodico
Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of duchenne's and becker muscular dystrophies of different ages (1991)
Vainzof, Mariz ; Pavanello, R C M; Pavanello Filho, I; Tsanaclis, Ana Maria Crous; Levy, J A; Passos-Bueno, Maria Rita ; Rapaport, D; Zatz, Mayana
Source: Neuromuscular Disorders. Unidades: FM, IB
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of duchenne's and becker muscular dystrophies of different ages. Neuromuscular Disorders, v. 1 , n. 3 , p. 177-83, 1991Tradução . . Disponível em: https://doi.org/10.1016/0960-8966(91)90022-k. Acesso em: 14 ago. 2024.
APA
Vainzof, M., Pavanello, R. C. M., Pavanello Filho, I., Tsanaclis, A. M. C., Levy, J. A., Passos-Bueno, M. R., et al. (1991). Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of duchenne's and becker muscular dystrophies of different ages. Neuromuscular Disorders, 1 ( 3 ), 177-83. doi:10.1016/0960-8966(91)90022-k
NLM
Vainzof M, Pavanello RCM, Pavanello Filho I, Tsanaclis AMC, Levy JA, Passos-Bueno MR, Rapaport D, Zatz M. Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of duchenne's and becker muscular dystrophies of different ages [Internet]. Neuromuscular Disorders. 1991 ;1 ( 3 ): 177-83.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/0960-8966(91)90022-k
Vancouver
Vainzof M, Pavanello RCM, Pavanello Filho I, Tsanaclis AMC, Levy JA, Passos-Bueno MR, Rapaport D, Zatz M. Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of duchenne's and becker muscular dystrophies of different ages [Internet]. Neuromuscular Disorders. 1991 ;1 ( 3 ): 177-83.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/0960-8966(91)90022-k
Artigo de periodico
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27 (1991)
Passos-Bueno, Maria Rita ; Byth, B; Love, D; Terwilliger, J; Ott, J; Rapaport, D; Vainzof, Mariz ; Zatz, Mayana ; Davies, K E
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
PASSOS-BUENO, Maria Rita et al. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27. Journal of the Neurological Sciences, v. 102, p. 206-8, 1991Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(91)90070-n. Acesso em: 14 ago. 2024.
APA
Passos-Bueno, M. R., Byth, B., Love, D., Terwilliger, J., Ott, J., Rapaport, D., et al. (1991). Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27. Journal of the Neurological Sciences, 102, 206-8. doi:10.1016/0022-510x(91)90070-n
NLM
Passos-Bueno MR, Byth B, Love D, Terwilliger J, Ott J, Rapaport D, Vainzof M, Zatz M, Davies KE. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27 [Internet]. Journal of the Neurological Sciences. 1991 ;102 206-8.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/0022-510x(91)90070-n
Vancouver
Passos-Bueno MR, Byth B, Love D, Terwilliger J, Ott J, Rapaport D, Vainzof M, Zatz M, Davies KE. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27 [Internet]. Journal of the Neurological Sciences. 1991 ;102 206-8.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/0022-510x(91)90070-n
Artigo de periodico
Limb-girdle syndrome: a genetic study of 22 large brazilian families comparison with x-linked duchenne and becker dystrophies (1991)
Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Pavanello, R C M; Pavanello Filho, I; Lima, M A B O; Zatz, Mayana
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
PASSOS-BUENO, Maria Rita et al. Limb-girdle syndrome: a genetic study of 22 large brazilian families comparison with x-linked duchenne and becker dystrophies. Journal of the Neurological Sciences, v. 103, p. 65-75, 1991Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(91)90286-g. Acesso em: 14 ago. 2024.
APA
Passos-Bueno, M. R., Vainzof, M., Pavanello, R. C. M., Pavanello Filho, I., Lima, M. A. B. O., & Zatz, M. (1991). Limb-girdle syndrome: a genetic study of 22 large brazilian families comparison with x-linked duchenne and becker dystrophies. Journal of the Neurological Sciences, 103, 65-75. doi:10.1016/0022-510x(91)90286-g
NLM
Passos-Bueno MR, Vainzof M, Pavanello RCM, Pavanello Filho I, Lima MABO, Zatz M. Limb-girdle syndrome: a genetic study of 22 large brazilian families comparison with x-linked duchenne and becker dystrophies [Internet]. Journal of the Neurological Sciences. 1991 ;103 65-75.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/0022-510x(91)90286-g
Vancouver
Passos-Bueno MR, Vainzof M, Pavanello RCM, Pavanello Filho I, Lima MABO, Zatz M. Limb-girdle syndrome: a genetic study of 22 large brazilian families comparison with x-linked duchenne and becker dystrophies [Internet]. Journal of the Neurological Sciences. 1991 ;103 65-75.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/0022-510x(91)90286-g

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