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Artigo de periodico
Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? (1993)
Passos-Bueno, Maria Rita ; Byth, B C; Rosemberg, Sérgio; Takata, R I; Bakker, E; Beggs, A H; Pavanello, R C M; Vainzof, Mariz ; Davies, K E; Zatz, Mayana
Source: American 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
PASSOS-BUENO, Maria Rita et al. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation?. American Journal of Medical Genetics, v. 46, n. 2 , p. 172-5, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460214. Acesso em: 03 nov. 2024.
APA
Passos-Bueno, M. R., Byth, B. C., Rosemberg, S., Takata, R. I., Bakker, E., Beggs, A. H., et al. (1993). Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? American Journal of Medical Genetics, 46( 2 ), 172-5. doi:10.1002/ajmg.1320460214
NLM
Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.1320460214
Vancouver
Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.1320460214
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: 03 nov. 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 nov. 03 ]
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 nov. 03 ]
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: 03 nov. 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 nov. 03 ] 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 nov. 03 ] Available from: https://doi.org/10.1002/ajmg.1320380130
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: 03 nov. 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 nov. 03 ] 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 nov. 03 ] Available from: https://doi.org/10.1016/0022-510x(91)90070-n
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 03 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. 03 ]
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. 03 ]
Artigo de periodico
Screening of delections in the dystrophin gene with the cdna probes cf23a, cf56a, and cf115 (1990)
Passos-Bueno, Maria Rita ; Rapaport, D; Love, D; Flint, T; Bortolini, E R; Zatz, Mayana ; Davies, K E
Source: 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. Screening of delections in the dystrophin gene with the cdna probes cf23a, cf56a, and cf115. Journal of Medical Genetics, v. 27, n. 3 , p. 145-50, 1990Tradução . . Acesso em: 03 nov. 2024.
APA
Passos-Bueno, M. R., Rapaport, D., Love, D., Flint, T., Bortolini, E. R., Zatz, M., & Davies, K. E. (1990). Screening of delections in the dystrophin gene with the cdna probes cf23a, cf56a, and cf115. Journal of Medical Genetics, 27( 3 ), 145-50.
NLM
Passos-Bueno MR, Rapaport D, Love D, Flint T, Bortolini ER, Zatz M, Davies KE. Screening of delections in the dystrophin gene with the cdna probes cf23a, cf56a, and cf115. Journal of Medical Genetics. 1990 ;27( 3 ): 145-50.[citado 2024 nov. 03 ]
Vancouver
Passos-Bueno MR, Rapaport D, Love D, Flint T, Bortolini ER, Zatz M, Davies KE. Screening of delections in the dystrophin gene with the cdna probes cf23a, cf56a, and cf115. Journal of Medical Genetics. 1990 ;27( 3 ): 145-50.[citado 2024 nov. 03 ]

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