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Trabalho de evento-resumo
Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation (2019)
Naslavsky, Michel ; Yamamoto, Guilherme Lopes ; Scliar, M. O; Wang, J; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Abstracts. Conference titles: ASHG Annual Meeting. Unidades: EE, IB, BIOINFORMÁTICA, FM
Subjects: GENÉTICA, IDOSOS
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ABNT
NASLAVSKY, Michel et al. Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation. 2019, Anais.. Houston: Escola de Enfermagem, Universidade de São Paulo, 2019. Disponível em: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf. Acesso em: 19 nov. 2024.
APA
Naslavsky, M., Yamamoto, G. L., Scliar, M. O., Wang, J., Duarte, Y. A. de O., Passos-Bueno, M. R., & Zatz, M. (2019). Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation. In Abstracts. Houston: Escola de Enfermagem, Universidade de São Paulo. Recuperado de https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
NLM
Naslavsky M, Yamamoto GL, Scliar MO, Wang J, Duarte YA de O, Passos-Bueno MR, Zatz M. Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation [Internet]. Abstracts. 2019 ;[citado 2024 nov. 19 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Vancouver
Naslavsky M, Yamamoto GL, Scliar MO, Wang J, Duarte YA de O, Passos-Bueno MR, Zatz M. Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation [Internet]. Abstracts. 2019 ;[citado 2024 nov. 19 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Trabalho de evento-resumo
Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? (2018)
Naslavsky, Michel ; Yamamoto, Guilherme Lopes ; Ezquina, Suzana ; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Abstracts. Conference titles: ASHI Annual Meeting. Unidades: EE, IB, FM, BIOINFORMÁTICA
Subjects: NEOPLASIAS, IDOSOS, SEQUENCIAMENTO GENÉTICO
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ABNT
NASLAVSKY, Michel et al. Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? 2018, Anais.. Baltimore: Escola de Enfermagem, Universidade de São Paulo, 2018. . Acesso em: 19 nov. 2024.
APA
Naslavsky, M., Yamamoto, G. L., Ezquina, S., Duarte, Y. A. de O., Passos-Bueno, M. R., & Zatz, M. (2018). Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? In Abstracts. Baltimore: Escola de Enfermagem, Universidade de São Paulo.
NLM
Naslavsky M, Yamamoto GL, Ezquina S, Duarte YA de O, Passos-Bueno MR, Zatz M. Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? Abstracts. 2018 ;[citado 2024 nov. 19 ]
Vancouver
Naslavsky M, Yamamoto GL, Ezquina S, Duarte YA de O, Passos-Bueno MR, Zatz M. Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? Abstracts. 2018 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Evaluation of the potential therapeutic use of immature stem cells in a canine model for duchenne muscular dystrophy (2007)
Ambrósio, Carlos Eduardo; Kerkis, I; Martins, D. S; Kerkis, A; Vanizof, M; Fonseca, S. A. S; Maranduba, C; Cabral, R. M; Peixoto, T. G; Morini, Adriana Caroprezo; Brólio, Roberto; Bertolini, L. R; Miglino, Maria Angélica; Zatz, Mayana
Source: Abstracts. Conference titles: International Federation of Placenta Association Meeting. Unidades: FMVZ, IB
Subjects: CÃES, CÉLULAS, DISTROFIA MUSCULAR ANIMAL
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ABNT
AMBRÓSIO, Carlos Eduardo et al. Evaluation of the potential therapeutic use of immature stem cells in a canine model for duchenne muscular dystrophy. 2007, Anais.. Kingston: Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, 2007. . Acesso em: 19 nov. 2024.
APA
Ambrósio, C. E., Kerkis, I., Martins, D. S., Kerkis, A., Vanizof, M., Fonseca, S. A. S., et al. (2007). Evaluation of the potential therapeutic use of immature stem cells in a canine model for duchenne muscular dystrophy. In Abstracts. Kingston: Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo.
NLM
Ambrósio CE, Kerkis I, Martins DS, Kerkis A, Vanizof M, Fonseca SAS, Maranduba C, Cabral RM, Peixoto TG, Morini AC, Brólio R, Bertolini LR, Miglino MA, Zatz M. Evaluation of the potential therapeutic use of immature stem cells in a canine model for duchenne muscular dystrophy. Abstracts. 2007 ;[citado 2024 nov. 19 ]
Vancouver
Ambrósio CE, Kerkis I, Martins DS, Kerkis A, Vanizof M, Fonseca SAS, Maranduba C, Cabral RM, Peixoto TG, Morini AC, Brólio R, Bertolini LR, Miglino MA, Zatz M. Evaluation of the potential therapeutic use of immature stem cells in a canine model for duchenne muscular dystrophy. Abstracts. 2007 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Reproductive analyzes in male golden retriever dogs affected by muscular dystrophy (GRMD) (2004)
Martins, D. S; Ambrósio, Carlos Eduardo; Gramado, A. P; Lima, A. R; Samoto, V. Y; Vannucchi, Camila Infantosi ; Simões, D. M. N; Ferreira, G. J. B; Giglio, R. R; Morini, A. C; Branco, E. R; Casagrande, C; Carvalho, M. B; Assumpção, Mayra Elena Ortiz D'Ávila ; Silva, T. J. C; Zucconi, E; kanayama, L. M; Miglino, Maria Angélica; Zatz, Mayana
Source: Abstracts. Conference titles: International Symposium on Canine and Feline Reproduction. Unidades: FMVZ, IB
Subjects: CÃES, DISTROFIA MUSCULAR ANIMAL
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ABNT
MARTINS, D. S et al. Reproductive analyzes in male golden retriever dogs affected by muscular dystrophy (GRMD). 2004, Anais.. Botucatu: Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, 2004. . Acesso em: 19 nov. 2024.
APA
Martins, D. S., Ambrósio, C. E., Gramado, A. P., Lima, A. R., Samoto, V. Y., Vannucchi, C. I., et al. (2004). Reproductive analyzes in male golden retriever dogs affected by muscular dystrophy (GRMD). In Abstracts. Botucatu: Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo.
NLM
Martins DS, Ambrósio CE, Gramado AP, Lima AR, Samoto VY, Vannucchi CI, Simões DMN, Ferreira GJB, Giglio RR, Morini AC, Branco ER, Casagrande C, Carvalho MB, Assumpção MEOD'Á, Silva TJC, Zucconi E, kanayama LM, Miglino MA, Zatz M. Reproductive analyzes in male golden retriever dogs affected by muscular dystrophy (GRMD). Abstracts. 2004 ;[citado 2024 nov. 19 ]
Vancouver
Martins DS, Ambrósio CE, Gramado AP, Lima AR, Samoto VY, Vannucchi CI, Simões DMN, Ferreira GJB, Giglio RR, Morini AC, Branco ER, Casagrande C, Carvalho MB, Assumpção MEOD'Á, Silva TJC, Zucconi E, kanayama LM, Miglino MA, Zatz M. Reproductive analyzes in male golden retriever dogs affected by muscular dystrophy (GRMD). Abstracts. 2004 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo periodico
Gender differences in the genetic determinants to alcohol dependence (2002)
Zatz, Mayana ; Guindalini, Camila; Scivoletto, Sandra; Ferreira, R. G. M.; Nishimura, A.; Ziberman, M.; Peluso, Marco Aurélio
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Assunto: ALCOOLISMO
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ABNT
ZATZ, Mayana et al. Gender differences in the genetic determinants to alcohol dependence. Abstracts. Baltimore: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 nov. 2024. , 2002
APA
Zatz, M., Guindalini, C., Scivoletto, S., Ferreira, R. G. M., Nishimura, A., Ziberman, M., & Peluso, M. A. (2002). Gender differences in the genetic determinants to alcohol dependence. Abstracts. Baltimore: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Guindalini C, Scivoletto S, Ferreira RGM, Nishimura A, Ziberman M, Peluso MA. Gender differences in the genetic determinants to alcohol dependence. Abstracts. 2002 ; 71( 4): 471 res.1763.[citado 2024 nov. 19 ]
Vancouver
Zatz M, Guindalini C, Scivoletto S, Ferreira RGM, Nishimura A, Ziberman M, Peluso MA. Gender differences in the genetic determinants to alcohol dependence. Abstracts. 2002 ; 71( 4): 471 res.1763.[citado 2024 nov. 19 ]
Trabalho de evento-resumo periodico
Is there an association between deletions/point mutations in the dystrophin gene and mental impaiment in Duchenne/Becker patients? (2002)
Vagenas, Dulci do Nascimento Fonseca; Cerqueira, A M P; Torres, A.; Pavanello, Rita de Cássia M.; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Assunto: DISTROFIA MUSCULAR
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ABNT
VAGENAS, Dulci do Nascimento Fonseca et al. Is there an association between deletions/point mutations in the dystrophin gene and mental impaiment in Duchenne/Becker patients?. Abstracts. Baltimore: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 nov. 2024. , 2002
APA
Vagenas, D. do N. F., Cerqueira, A. M. P., Torres, A., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (2002). Is there an association between deletions/point mutations in the dystrophin gene and mental impaiment in Duchenne/Becker patients? Abstracts. Baltimore: Instituto de Biociências, Universidade de São Paulo.
NLM
Vagenas D do NF, Cerqueira AMP, Torres A, Pavanello R de CM, Passos-Bueno MR, Zatz M. Is there an association between deletions/point mutations in the dystrophin gene and mental impaiment in Duchenne/Becker patients? Abstracts. 2002 ; 71( 4): 525 res.2083.[citado 2024 nov. 19 ]
Vancouver
Vagenas D do NF, Cerqueira AMP, Torres A, Pavanello R de CM, Passos-Bueno MR, Zatz M. Is there an association between deletions/point mutations in the dystrophin gene and mental impaiment in Duchenne/Becker patients? Abstracts. 2002 ; 71( 4): 525 res.2083.[citado 2024 nov. 19 ]
Trabalho de evento-resumo periodico
Another locus for autosomal dominant late onset Alzheimers disease in brazilian families? (2002)
Nishimura, A. L.; Oliveira, J. R. M.; Brito-Marques, Paulo Roberto; Nitrini, Ricardo; Bertolucci, P. H.; Okamoto, Ivan H.; Zatz, Mayana
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: IB, FM
Subjects: DOENÇAS CEREBRAIS, DOENÇAS GENÉTICAS, DEMÊNCIA
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ABNT
NISHIMURA, A. L. et al. Another locus for autosomal dominant late onset Alzheimers disease in brazilian families?. Abstracts. Baltimore: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 nov. 2024. , 2002
APA
Nishimura, A. L., Oliveira, J. R. M., Brito-Marques, P. R., Nitrini, R., Bertolucci, P. H., Okamoto, I. H., & Zatz, M. (2002). Another locus for autosomal dominant late onset Alzheimers disease in brazilian families? Abstracts. Baltimore: Instituto de Biociências, Universidade de São Paulo.
NLM
Nishimura AL, Oliveira JRM, Brito-Marques PR, Nitrini R, Bertolucci PH, Okamoto IH, Zatz M. Another locus for autosomal dominant late onset Alzheimers disease in brazilian families? Abstracts. 2002 ; 71( 4): suppl. 480 res.1814.[citado 2024 nov. 19 ]
Vancouver
Nishimura AL, Oliveira JRM, Brito-Marques PR, Nitrini R, Bertolucci PH, Okamoto IH, Zatz M. Another locus for autosomal dominant late onset Alzheimers disease in brazilian families? Abstracts. 2002 ; 71( 4): suppl. 480 res.1814.[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b) (1996)
Bushby, K; Bashir, R; Britton, S; Keers, S; Mahjneh, I; Zatz, Mayana ; Strachan, T
Source: Abstracts. Conference titles: Limb Girdle Muscular Dystrophies Genetics Workshop. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
BUSHBY, K et al. Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b). 1996, Anais.. Tunis: Instituto de Biociências, Universidade de São Paulo, 1996. . Acesso em: 19 nov. 2024.
APA
Bushby, K., Bashir, R., Britton, S., Keers, S., Mahjneh, I., Zatz, M., & Strachan, T. (1996). Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b). In Abstracts. Tunis: Instituto de Biociências, Universidade de São Paulo.
NLM
Bushby K, Bashir R, Britton S, Keers S, Mahjneh I, Zatz M, Strachan T. Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b). Abstracts. 1996 ;[citado 2024 nov. 19 ]
Vancouver
Bushby K, Bashir R, Britton S, Keers S, Mahjneh I, Zatz M, Strachan T. Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b). Abstracts. 1996 ;[citado 2024 nov. 19 ]
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
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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: 19 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. 19 ]
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. 19 ]
Trabalho de evento-resumo
Genomic screening for beta and gamma-sarcoglycan gene mutations (1996)
Bonnemann, C G; Mcnally, E M; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Moreira, E S; Pavanello, R C M; Marie, Suely Kazue Nagahashi; Othmane, K B; Denton, P H; Vance, J M; Noguchi, S; Ozawa, E
Source: Abstracts. Conference titles: Limb Girdle Muscular Dystrophies Genetics Workshop. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
BONNEMANN, C G et al. Genomic screening for beta and gamma-sarcoglycan gene mutations. 1996, Anais.. Tunis: Instituto de Biociências, Universidade de São Paulo, 1996. . Acesso em: 19 nov. 2024.
APA
Bonnemann, C. G., Mcnally, E. M., Passos-Bueno, M. R., Vainzof, M., Moreira, E. S., Pavanello, R. C. M., et al. (1996). Genomic screening for beta and gamma-sarcoglycan gene mutations. In Abstracts. Tunis: Instituto de Biociências, Universidade de São Paulo.
NLM
Bonnemann CG, Mcnally EM, Passos-Bueno MR, Vainzof M, Moreira ES, Pavanello RCM, Marie SKN, Othmane KB, Denton PH, Vance JM, Noguchi S, Ozawa E. Genomic screening for beta and gamma-sarcoglycan gene mutations. Abstracts. 1996 ;[citado 2024 nov. 19 ]
Vancouver
Bonnemann CG, Mcnally EM, Passos-Bueno MR, Vainzof M, Moreira ES, Pavanello RCM, Marie SKN, Othmane KB, Denton PH, Vance JM, Noguchi S, Ozawa E. Genomic screening for beta and gamma-sarcoglycan gene mutations. Abstracts. 1996 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy (lgmd 2b) (1996)
Mahjneh, L; Passos-Bueno, Maria Rita ; Zatz, Mayana ; Vainzof, Mariz ; Marconi, G; Nashef, L; Bashir, R; Bushby, K
Source: Abstracts. Conference titles: Limb Girdle Muscular Dystrophies Genetics Workshop. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
MAHJNEH, L et al. Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy (lgmd 2b). 1996, Anais.. Tunis: Instituto de Biociências, Universidade de São Paulo, 1996. . Acesso em: 19 nov. 2024.
APA
Mahjneh, L., Passos-Bueno, M. R., Zatz, M., Vainzof, M., Marconi, G., Nashef, L., et al. (1996). Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy (lgmd 2b). In Abstracts. Tunis: Instituto de Biociências, Universidade de São Paulo.
NLM
Mahjneh L, Passos-Bueno MR, Zatz M, Vainzof M, Marconi G, Nashef L, Bashir R, Bushby K. Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy (lgmd 2b). Abstracts. 1996 ;[citado 2024 nov. 19 ]
Vancouver
Mahjneh L, Passos-Bueno MR, Zatz M, Vainzof M, Marconi G, Nashef L, Bashir R, Bushby K. Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy (lgmd 2b). Abstracts. 1996 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Immunohistochemical dystrophin study of duchenne dystrophy with the concomitant use of the n-terminal and c-terminal antibodies (1990)
Vainzof, Mariz ; Pavanello, R C M; Rapaport, D; Passos-Bueno, Maria Rita ; Zubrzycka-Gaarn, E E; Hoffman, E; Zatz, Mayana
Source: Abstracts. Conference titles: International Congress on Neuromuscular Diseases. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
VAINZOF, Mariz et al. Immunohistochemical dystrophin study of duchenne dystrophy with the concomitant use of the n-terminal and c-terminal antibodies. 1990, Anais.. Munich: Instituto de Biociências, Universidade de São Paulo, 1990. . Acesso em: 19 nov. 2024.
APA
Vainzof, M., Pavanello, R. C. M., Rapaport, D., Passos-Bueno, M. R., Zubrzycka-Gaarn, E. E., Hoffman, E., & Zatz, M. (1990). Immunohistochemical dystrophin study of duchenne dystrophy with the concomitant use of the n-terminal and c-terminal antibodies. In Abstracts. Munich: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Pavanello RCM, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Hoffman E, Zatz M. Immunohistochemical dystrophin study of duchenne dystrophy with the concomitant use of the n-terminal and c-terminal antibodies. Abstracts. 1990 ;[citado 2024 nov. 19 ]
Vancouver
Vainzof M, Pavanello RCM, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Hoffman E, Zatz M. Immunohistochemical dystrophin study of duchenne dystrophy with the concomitant use of the n-terminal and c-terminal antibodies. Abstracts. 1990 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Screening of dna deletions in duchenne dystrophy (dmd) through mental retardation (1990)
Rapaport, D; Passos-Bueno, Maria Rita ; Brandao, L; Vainzof, Mariz ; Lima, M A B O; Zatz, Mayana
Source: Abstracts. Conference titles: International Congress on Neuromuscular Diseases. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
RAPAPORT, D et al. Screening of dna deletions in duchenne dystrophy (dmd) through mental retardation. 1990, Anais.. Munich: Instituto de Biociências, Universidade de São Paulo, 1990. . Acesso em: 19 nov. 2024.
APA
Rapaport, D., Passos-Bueno, M. R., Brandao, L., Vainzof, M., Lima, M. A. B. O., & Zatz, M. (1990). Screening of dna deletions in duchenne dystrophy (dmd) through mental retardation. In Abstracts. Munich: Instituto de Biociências, Universidade de São Paulo.
NLM
Rapaport D, Passos-Bueno MR, Brandao L, Vainzof M, Lima MABO, Zatz M. Screening of dna deletions in duchenne dystrophy (dmd) through mental retardation. Abstracts. 1990 ;[citado 2024 nov. 19 ]
Vancouver
Rapaport D, Passos-Bueno MR, Brandao L, Vainzof M, Lima MABO, Zatz M. Screening of dna deletions in duchenne dystrophy (dmd) through mental retardation. Abstracts. 1990 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh) (1990)
Passos-Bueno, Maria Rita ; Love, D; Byth, B; Terwillinger, J; Rapaport, D; Davies, K E; Zatz, Mayana
Source: Abstracts. Conference titles: International Congress on Neuromuscular Diseases. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
PASSOS-BUENO, Maria Rita et al. Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh). 1990, Anais.. Munich: Instituto de Biociências, Universidade de São Paulo, 1990. . Acesso em: 19 nov. 2024.
APA
Passos-Bueno, M. R., Love, D., Byth, B., Terwillinger, J., Rapaport, D., Davies, K. E., & Zatz, M. (1990). Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh). In Abstracts. Munich: Instituto de Biociências, Universidade de São Paulo.
NLM
Passos-Bueno MR, Love D, Byth B, Terwillinger J, Rapaport D, Davies KE, Zatz M. Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh). Abstracts. 1990 ;[citado 2024 nov. 19 ]
Vancouver
Passos-Bueno MR, Love D, Byth B, Terwillinger J, Rapaport D, Davies KE, Zatz M. Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh). Abstracts. 1990 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Recurrence of duchenne dystrophy through non-maternal lines in four genealogies (1990)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Rapaport, D; Vainzof, Mariz
Source: Abstracts. Conference titles: International Congress of Neuromuscular Diseases. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
ZATZ, Mayana et al. Recurrence of duchenne dystrophy through non-maternal lines in four genealogies. 1990, Anais.. Munich: Instituto de Biociências, Universidade de São Paulo, 1990. . Acesso em: 19 nov. 2024.
APA
Zatz, M., Passos-Bueno, M. R., Rapaport, D., & Vainzof, M. (1990). Recurrence of duchenne dystrophy through non-maternal lines in four genealogies. In Abstracts. Munich: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M. Recurrence of duchenne dystrophy through non-maternal lines in four genealogies. Abstracts. 1990 ;[citado 2024 nov. 19 ]
Vancouver
Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M. Recurrence of duchenne dystrophy through non-maternal lines in four genealogies. Abstracts. 1990 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
X-autosome translocations in females with X-linked recessive diseases (1986)
Vianna-Morgante, Angela M ; Batista, D A S; Levisky, R; Zatz, Mayana
Source: Abstracts. Conference titles: International Congress of Human Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, CROMOSSOMO X, BIOLOGIA CELULAR
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ABNT
VIANNA-MORGANTE, Angela M et al. X-autosome translocations in females with X-linked recessive diseases. 1986, Anais.. Berlin: Instituto de Biociências, Universidade de São Paulo, 1986. . Acesso em: 19 nov. 2024.
APA
Vianna-Morgante, A. M., Batista, D. A. S., Levisky, R., & Zatz, M. (1986). X-autosome translocations in females with X-linked recessive diseases. In Abstracts. Berlin: Instituto de Biociências, Universidade de São Paulo.
NLM
Vianna-Morgante AM, Batista DAS, Levisky R, Zatz M. X-autosome translocations in females with X-linked recessive diseases. Abstracts. 1986 ;[citado 2024 nov. 19 ]
Vancouver
Vianna-Morgante AM, Batista DAS, Levisky R, Zatz M. X-autosome translocations in females with X-linked recessive diseases. Abstracts. 1986 ;[citado 2024 nov. 19 ]

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