The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis (1998)
- Authors:
- USP affiliated authors: ZATZ, MAYANA - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; MARIE, SUELY KAZUE NAGAHASHI - FM
- Unidades: IB; FM
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Conference Handbook and Speaker Papers
- Conference titles: Facioscapulohumeral Muscular Dystrophy Meeting
-
ABNT
ZATZ, Mayana et al. The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. 1998, Anais.. Sydney: Instituto de Biociências, Universidade de São Paulo, 1998. . Acesso em: 19 set. 2024. -
APA
Zatz, M., Marie, S. K. N., Cerqueira, A. M. P., Vainzof, M., Pavanello, R. de C. M., & Passos-Bueno, M. R. (1998). The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. In Conference Handbook and Speaker Papers. Sydney: Instituto de Biociências, Universidade de São Paulo. -
NLM
Zatz M, Marie SKN, Cerqueira AMP, Vainzof M, Pavanello R de CM, Passos-Bueno MR. The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. Conference Handbook and Speaker Papers. 1998 ;[citado 2024 set. 19 ] -
Vancouver
Zatz M, Marie SKN, Cerqueira AMP, Vainzof M, Pavanello R de CM, Passos-Bueno MR. The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis. Conference Handbook and Speaker Papers. 1998 ;[citado 2024 set. 19 ] - Estudo populacional das ataxias espinocerebelares na população brasileira
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- Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex
- Mecanismo molecular da distrofia muscular fácio-escápulo-humeral: ainda uma incógnita!
- Análise molecular de pacientes brasileiros com ataxia espinocerebelar
- Estudo molecular das neuropatias periféricas hereditárias - CMT1A e HNPP
- Clinical and molecular analysis of spinal muscular atrophy in brazilian patients
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