Anticipation revisited in facioscapulohumeral muscular dystrophy (2003)
- Authors:
- USP affiliated authors: ZATZ, MAYANA - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidade: IB
- Assunto: DISTROFIA MUSCULAR
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Neuromuscular Disorders
- Volume/Número/Paginação/Ano: v. 13, n. 7-8, p. 633, 2003
- Conference titles: International Congress of the World Muscle Society
-
ABNT
ZATZ, Mayana et al. Anticipation revisited in facioscapulohumeral muscular dystrophy. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 abr. 2023. , 2003 -
APA
Zatz, M., Tonini, M. M. O., Cerqueira, A. M. P., Pavanello, R. de C. M., & Passos-Bueno, M. R. (2003). Anticipation revisited in facioscapulohumeral muscular dystrophy. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. -
NLM
Zatz M, Tonini MMO, Cerqueira AMP, Pavanello R de CM, Passos-Bueno MR. Anticipation revisited in facioscapulohumeral muscular dystrophy. Neuromuscular Disorders. 2003 ; 13( 7-8): 633.[citado 2023 abr. 01 ] -
Vancouver
Zatz M, Tonini MMO, Cerqueira AMP, Pavanello R de CM, Passos-Bueno MR. Anticipation revisited in facioscapulohumeral muscular dystrophy. Neuromuscular Disorders. 2003 ; 13( 7-8): 633.[citado 2023 abr. 01 ] - Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
- Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
- Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- 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
- 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
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas