Genetic and linkage analysis in autosomal recessive limb-girdle muscular dystrophy (1996)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Publisher: Marcel Dekker
- Publisher place: New York
- Date published: 1996
- Source:
- Título do periódico: Handbook of Muscle Disease
-
ABNT
PASSOS-BUENO, Maria Rita e VAINZOF, Mariz e ZATZ, Mayana. Genetic and linkage analysis in autosomal recessive limb-girdle muscular dystrophy. Handbook of Muscle Disease. Tradução . New York: Marcel Dekker, 1996. . . Acesso em: 04 ago. 2024. -
APA
Passos-Bueno, M. R., Vainzof, M., & Zatz, M. (1996). Genetic and linkage analysis in autosomal recessive limb-girdle muscular dystrophy. In Handbook of Muscle Disease. New York: Marcel Dekker. -
NLM
Passos-Bueno MR, Vainzof M, Zatz M. Genetic and linkage analysis in autosomal recessive limb-girdle muscular dystrophy. In: Handbook of Muscle Disease. New York: Marcel Dekker; 1996. [citado 2024 ago. 04 ] -
Vancouver
Passos-Bueno MR, Vainzof M, Zatz M. Genetic and linkage analysis in autosomal recessive limb-girdle muscular dystrophy. In: Handbook of Muscle Disease. New York: Marcel Dekker; 1996. [citado 2024 ago. 04 ] - 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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