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:
- Conference titles: Facioscapulohumeral Muscular Dystrophy Meeting
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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: 27 dez. 2025. -
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 2025 dez. 27 ] -
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 2025 dez. 27 ] - Estudo molecular de neuropatias periféricas - CMT1A e HNPP
- The limb-girdle muscular dystrophy 2G (LGMD2G) phenotype
- Estudo molecular da neuropatia de Charcot-Marie-Tooth tipo 1 (CMT1) e neuropatia hereditária com paralisias por compressão (HNPP)
- Autosomal dominant pure spastic paraplegia in a brazilian family: linkage to chromosome 8q and study of muscle syntrophin 'beta'1
- A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies
- Estudo populacional das ataxias espinocerebelares na população brasileira
- Sarcoglicanopatias na população brasileira
- Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI)
- Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population
- Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex
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