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Artigo de periodico
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 brazilian families (1996)
Passos-Bueno, Maria Rita ; Moreira, E S; Marie, Suely Kazue Nagahashi; Bashir, R; Vasquez, L; Love, D R; Vainzof, Mariz ; Iughetti, P; Oliveira, J. R.; Bakker, E; Strachan, T
Source: Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
PASSOS-BUENO, Maria Rita et al. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 brazilian families. Journal of Medical Genetics, v. 33, p. 97-102, 1996Tradução . . Disponível em: https://doi.org/10.1136/jmg.33.2.97. Acesso em: 10 jun. 2024.
APA
Passos-Bueno, M. R., Moreira, E. S., Marie, S. K. N., Bashir, R., Vasquez, L., Love, D. R., et al. (1996). Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 brazilian families. Journal of Medical Genetics, 33, 97-102. doi:10.1136/jmg.33.2.97
NLM
Passos-Bueno MR, Moreira ES, Marie SKN, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 brazilian families [Internet]. Journal of Medical Genetics. 1996 ;33 97-102.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1136/jmg.33.2.97
Vancouver
Passos-Bueno MR, Moreira ES, Marie SKN, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 brazilian families [Internet]. Journal of Medical Genetics. 1996 ;33 97-102.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1136/jmg.33.2.97
Trabalho de evento-resumo
Clinical and laboratorial findings in autosomal recessive muscular dystrophies (armd) (1995)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Marie, Suely Kazue Nagahashi; Moreira, E S; Bashir, R; Vasquez, L; Love, D R; Iughetti, P; Oliveira, J. R.; Bakker, E; Strachan, T; Bushby, K
Conference titles: European Neuro Muscular Center International Workshop. Unidade: IB
Subjects: GENÉTICA MÉDICA, NEUROLOGIA
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ABNT
ZATZ, Mayana et al. Clinical and laboratorial findings in autosomal recessive muscular dystrophies (armd). 1995, Anais.. Naarden: Instituto de Biociências, Universidade de São Paulo, 1995. . Acesso em: 10 jun. 2024.
APA
Zatz, M., Passos-Bueno, M. R., Marie, S. K. N., Moreira, E. S., Bashir, R., Vasquez, L., et al. (1995). Clinical and laboratorial findings in autosomal recessive muscular dystrophies (armd). In . Naarden: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Passos-Bueno MR, Marie SKN, Moreira ES, Bashir R, Vasquez L, Love DR, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K. Clinical and laboratorial findings in autosomal recessive muscular dystrophies (armd). 1995 ;[citado 2024 jun. 10 ]
Vancouver
Zatz M, Passos-Bueno MR, Marie SKN, Moreira ES, Bashir R, Vasquez L, Love DR, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K. Clinical and laboratorial findings in autosomal recessive muscular dystrophies (armd). 1995 ;[citado 2024 jun. 10 ]
Artigo de periodico
Molecular characterization of further dystrophin gene microsatellites (1995)
King, S C; Roche, A L; Passos-Bueno, Maria Rita ; Takata, R I; Zatz, Mayana ; Cockburn, D J; Seller, A; Stapleton, P M; Love, D R
Source: Molecular and Cellular Probes. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KING, S C et al. Molecular characterization of further dystrophin gene microsatellites. Molecular and Cellular Probes, v. 9 , p. 361-70, 1995Tradução . . Disponível em: https://doi.org/10.1016/s0890-8508(95)91700-4. Acesso em: 10 jun. 2024.
APA
King, S. C., Roche, A. L., Passos-Bueno, M. R., Takata, R. I., Zatz, M., Cockburn, D. J., et al. (1995). Molecular characterization of further dystrophin gene microsatellites. Molecular and Cellular Probes, 9 , 361-70. doi:10.1016/s0890-8508(95)91700-4
NLM
King SC, Roche AL, Passos-Bueno MR, Takata RI, Zatz M, Cockburn DJ, Seller A, Stapleton PM, Love DR. Molecular characterization of further dystrophin gene microsatellites [Internet]. Molecular and Cellular Probes. 1995 ;9 361-70.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/s0890-8508(95)91700-4
Vancouver
King SC, Roche AL, Passos-Bueno MR, Takata RI, Zatz M, Cockburn DJ, Seller A, Stapleton PM, Love DR. Molecular characterization of further dystrophin gene microsatellites [Internet]. Molecular and Cellular Probes. 1995 ;9 361-70.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/s0890-8508(95)91700-4
Artigo de periodico
New dna marker, d6s129, identifies a hindiii polymorphism on chromosome 6q (1991)
Byth, B C; Love, D R; Passos-Bueno, Maria Rita ; Davies, K E
Source: Nucleic Acids Research. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BYTH, B C et al. New dna marker, d6s129, identifies a hindiii polymorphism on chromosome 6q. Nucleic Acids Research, v. 19, n. 15, p. 4310, 1991Tradução . . Acesso em: 10 jun. 2024.
APA
Byth, B. C., Love, D. R., Passos-Bueno, M. R., & Davies, K. E. (1991). New dna marker, d6s129, identifies a hindiii polymorphism on chromosome 6q. Nucleic Acids Research, 19( 15), 4310.
NLM
Byth BC, Love DR, Passos-Bueno MR, Davies KE. New dna marker, d6s129, identifies a hindiii polymorphism on chromosome 6q. Nucleic Acids Research. 1991 ;19( 15): 4310.[citado 2024 jun. 10 ]
Vancouver
Byth BC, Love DR, Passos-Bueno MR, Davies KE. New dna marker, d6s129, identifies a hindiii polymorphism on chromosome 6q. Nucleic Acids Research. 1991 ;19( 15): 4310.[citado 2024 jun. 10 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 10 jun. 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 jun. 10 ] 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 jun. 10 ] Available from: https://doi.org/10.1002/ajmg.1320380130

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