Clinical and laboratorial findings in autosomal recessive muscular dystrophies (armd) (1995)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Subjects: GENÉTICA MÉDICA; NEUROLOGIA
- Language: Inglês
- Imprenta:
- Conference titles: European Neuro Muscular Center International Workshop
-
ABNT
ZATZ, Mayana et al. Clinical and laboratorial findings in autosomal recessive muscular dystrophies (armd). 1995, Anais.. Naarden: Instituto de Biociências, Universidade de São Paulo, 1995. . Acesso em: 23 jul. 2024. -
APA
Zatz, M., Passos-Bueno, M. R., Marie, S. K. N., Moreira, E. S., Bashir, R., Vasquez, L., et al. (1995). Clinical and laboratorial findings in autosomal recessive muscular dystrophies (armd). In . Naarden: Instituto de Biociências, Universidade de São Paulo. -
NLM
Zatz M, Passos-Bueno MR, Marie SKN, Moreira ES, Bashir R, Vasquez L, Love DR, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K. Clinical and laboratorial findings in autosomal recessive muscular dystrophies (armd). 1995 ;[citado 2024 jul. 23 ] -
Vancouver
Zatz M, Passos-Bueno MR, Marie SKN, Moreira ES, Bashir R, Vasquez L, Love DR, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K. Clinical and laboratorial findings in autosomal recessive muscular dystrophies (armd). 1995 ;[citado 2024 jul. 23 ] - Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations
- A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3
- Mapping, cloning, and characterization of genes important for human development
- Deletion encompassing 50% of the coding region of the dystrophin gene is still compatible with a mild becker dystrophy (bmd) phenotype
- Mesma mutacao no gene da adalina pode causar formas graves e leves de distrofia muscular tipo cinturas
- Sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies (ar-lgmd)
- Phenotype of chromosome 2p-linked limb-girdle muscular dystrophy
- Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e)
- Mutações diferentes em pacientes com distrofia muscular do tipo duchenne pertencentes a uma mesma família
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