ReP USP - Resultado da busca

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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 23 maio 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 maio 23 ] 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 maio 23 ] Available from: https://doi.org/10.1002/ajmg.1320390414
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: 23 maio 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 maio 23 ] 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 maio 23 ] 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: 23 maio 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 maio 23 ]
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 maio 23 ]
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: 23 maio 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 maio 23 ]
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 maio 23 ]

USP Schools

ReP

Filtros

Authors