Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population (1996)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; CERQUEIRA, ANTONIA MARIA PEREIRA DE - IB ; ZATZ, MAYANA - IB
- Unidades: IB; IB; IB
- Subjects: BIOLOGIA MOLECULAR; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Program and Abstracts
- Conference title: Pabmb Congress
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ABNT
ZATZ, M; VAINZOF, M; MOREIRA, E S; et al. Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population. Anais.. Pucon: [s.n.], 1996. -
APA
Zatz, M., Vainzof, M., Moreira, E. S., Campiotto, S., Cerqueira, A. M. P., & Passos-Bueno, M. R. (1996). Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population. In Program and Abstracts. Pucon. -
NLM
Zatz M, Vainzof M, Moreira ES, Campiotto S, Cerqueira AMP, Passos-Bueno MR. Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population. Program and Abstracts. 1996 ; -
Vancouver
Zatz M, Vainzof M, Moreira ES, Campiotto S, Cerqueira AMP, Passos-Bueno MR. Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population. Program and Abstracts. 1996 ; - Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- High proportion of new mutations and possible anticipation in brazilian facioscapulohumeral muscular dystrophy families
- High proportion of new mutations and possible anticipation following molecular genetic studies in brazilian facioscapulohumeral muscular dystrophy (fshd) families
- Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
- Linkage analysis using 6q probes in facioscapulohumeral dystrophy (fsh)
- Distrofia tipo duchenne (dmd): estudo imunohistoquimico da distrofina atraves do uso concomitante de anticorpos n-terminal e c-terminal
- Triagem de pacientes com a forma autossomica recessiva de distrofia tipo duchene, atraves de estudos de distrifina e dna
- Uso de sondas homologas para identificacao de novos genes: a sequencia b3 como candidata para a sindrome de cinturas
- Ausencia de heterogeneidade genetica na distrofia muscular tipo facio-escapulo-humeral (fsh) atraves de estudos de ligacao
- Genetic risk estimates for duchenne dystrophy ( dmd )in the absence of dna deletions in the central region of the dystrophin gene
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