ReP USP - Resultado da busca

Filtros : "Takata, Reinaldo I" Removido: "Nogueira, Leticia" Limpar

Filtros

USP affiliated authors
- vainzof, mariz (~2)
- bueno, maria rita dos santos e passos (~1)
- zatz, mayana (~1)
Date published
- 2013 (~1)
- 1993 (~1)
Subjects
- cromossomo x (1)
- distrofia muscular (1)
- heterogeneidade (1)
- miopatias congênitas estruturais (1)
- mutação genética (1)

Language
- inglês (~2)
Source title
- american journal of medical genetics (~1)
- journal of molecular neuroscience (~1)
Publisher
Conference titles
GDS
Countries/Territories
- estados unidos (~2)
Grupo de pesquisa
Funding Agencies
- conselho nacional de desenvolvimento científico e tecnológico (cnpq) (~1)
- financiado pela abdim (~1)
- fundação de amparo à pesquisa do estado de são paulo (fapesp) (~1)
Indexado em
- indexado no: biological abstracts (online) (~2)
- indexado no: web of science (~2)
- indexado no: current contents (~1)
- indexado no: pubmed (~1)
- indexado no: scopus (~1)
Collaboration
Normalized affiliation
Non normalized affiliation
- departamento de pediatria, santa casa da miseric6rdia de ,são paulo, são paulo, brazil (1)
- department of human genetics, leiden university, the netherlands (1)
- electron microscopy department, sarah network of rehabilitation hospitals, brasília, brazil (1)
- genetics division, children’s hospital, harvard medical school, boston, massachusetts (1)
- institute of molecular medicine, university of oxford, england (1)

Artigo de periodico
Muscle phenotypic variability in limb girdle muscular dystrophy 2 G (2013)
Paim, Julia F; Cotta, Ana; Vargas, Antonio P; Navarro, Monica M; Valicek, Jaquelin; Carvalho, Elmano; da-Cunha-Junior, Antonio; Plentz, Estevão; Braz, Shelida v; Takata, Reinaldo I; Almeida, Camila F; Vainzof, Mariz
Source: Journal of Molecular Neuroscience. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, MIOPATIAS CONGÊNITAS ESTRUTURAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAIM, Julia F et al. Muscle phenotypic variability in limb girdle muscular dystrophy 2 G. Journal of Molecular Neuroscience, v. 50, n. 2, p. 339-344, 2013Tradução . . Disponível em: https://doi.org/10.1007/s12031-013-9987-6. Acesso em: 21 out. 2025.
APA
Paim, J. F., Cotta, A., Vargas, A. P., Navarro, M. M., Valicek, J., Carvalho, E., et al. (2013). Muscle phenotypic variability in limb girdle muscular dystrophy 2 G. Journal of Molecular Neuroscience, 50( 2), 339-344. doi:10.1007/s12031-013-9987-6
NLM
Paim JF, Cotta A, Vargas AP, Navarro MM, Valicek J, Carvalho E, da-Cunha-Junior A, Plentz E, Braz S v, Takata RI, Almeida CF, Vainzof M. Muscle phenotypic variability in limb girdle muscular dystrophy 2 G [Internet]. Journal of Molecular Neuroscience. 2013 ; 50( 2): 339-344.[citado 2025 out. 21 ] Available from: https://doi.org/10.1007/s12031-013-9987-6
Vancouver
Paim JF, Cotta A, Vargas AP, Navarro MM, Valicek J, Carvalho E, da-Cunha-Junior A, Plentz E, Braz S v, Takata RI, Almeida CF, Vainzof M. Muscle phenotypic variability in limb girdle muscular dystrophy 2 G [Internet]. Journal of Molecular Neuroscience. 2013 ; 50( 2): 339-344.[citado 2025 out. 21 ] Available from: https://doi.org/10.1007/s12031-013-9987-6
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, Barbara C; Rosenberg, Sergio; Takata, Reinaldo I; Bakker, Egbert ; Beggs, Alan H ; Pavanello, Rita C; Vainzof, Mariz ; Davies, Kay E; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: RETARDO MENTAL, HETEROGENEIDADE, CROMOSSOMO X
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, p. 172-175, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460214. Acesso em: 21 out. 2025.
APA
Passos-Bueno, M. R., Byth, B. C., Rosenberg, 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, 172-175. doi:10.1002/ajmg.1320460214
NLM
Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, 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 ; 46 172-175.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/ajmg.1320460214
Vancouver
Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, 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 ; 46 172-175.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/ajmg.1320460214

Digital Library of Intellectual Production of Universidade de São Paulo 2012 - 2025