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
- Unidade: IB
- Subjects: BIOLOGIA MOLECULAR; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Program and Abstracts
- Conference titles: Pabmb Congress
-
ABNT
ZATZ, M et al. Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population. 1996, Anais.. Pucon: Instituto de Biociências, Universidade de São Paulo, 1996. . Acesso em: 06 fev. 2023. -
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: Instituto de Biociências, Universidade de São Paulo. -
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 ;[citado 2023 fev. 06 ] -
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 ;[citado 2023 fev. 06 ] - Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
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- 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
- Reevalutation and fine mapping of a Brazilian pedigree reveals another family with Allan-Herndon-Dudley syndrome
- Anticipation revisited in facioscapulohumeral muscular dystrophy
- Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern DNA deletion. [Carta ao editor]
- Transposon-like element in the dystrophin gene. [Carta ao editor]
- A gene related to Caenorhabditis elegans spermatogenes is factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
- Sarcoglycanopathies and limb-girdle syndromes: diagnostic insights
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