Frequency and pattern of dna deletions in duchenne (dmd)and becker (bmd) patients: comparison of different racial background and isolated versus inherited cases (1992)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Subjects: GENÉTICA; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Publisher place: Ribeirao Preto
- Date published: 1992
- Source:
- Título do periódico: Revista Brasileira de Genetica = Brazilian Journal of Genetics
- Volume/Número/Paginação/Ano: v.15, n.2 , p.459-67, jun. 1992
-
ABNT
RAPAPORT, D et al. Frequency and pattern of dna deletions in duchenne (dmd)and becker (bmd) patients: comparison of different racial background and isolated versus inherited cases. Revista Brasileira de Genetica = Brazilian Journal of Genetics, v. 15, n. ju 1992, p. 459-67, 1992Tradução . . Acesso em: 25 abr. 2024. -
APA
Rapaport, D., Passos-Bueno, M. R., Vainzof, M., Lima, M. A. B. O., & Zatz, M. (1992). Frequency and pattern of dna deletions in duchenne (dmd)and becker (bmd) patients: comparison of different racial background and isolated versus inherited cases. Revista Brasileira de Genetica = Brazilian Journal of Genetics, 15( ju 1992), 459-67. -
NLM
Rapaport D, Passos-Bueno MR, Vainzof M, Lima MABO, Zatz M. Frequency and pattern of dna deletions in duchenne (dmd)and becker (bmd) patients: comparison of different racial background and isolated versus inherited cases. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1992 ;15( ju 1992): 459-67.[citado 2024 abr. 25 ] -
Vancouver
Rapaport D, Passos-Bueno MR, Vainzof M, Lima MABO, Zatz M. Frequency and pattern of dna deletions in duchenne (dmd)and becker (bmd) patients: comparison of different racial background and isolated versus inherited cases. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1992 ;15( ju 1992): 459-67.[citado 2024 abr. 25 ] - Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- 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
- Racial effect on serum creatine-kinase: implications for estimation of heterozygosity risks for females at-risk for Duchenne dystrophy
- Proportion of sca1 and machado-joseph (mjd / sca3) and different origins of mutations for the mjd / sca3 disease
- Positional cloning of a gene for autosomal recessive limb-girdle muscular dystrophy
- Is there an association between deletions/point mutations in the dystrophin gene and mental impaiment in Duchenne/Becker patients?
- A novel stop codon mutation in the PMP22 gene associated with a variable phenotype
- Mild and severe muscular dystrophy caused by a single 'GAMA'- sarcoglycan mutation
- Molecular and clinical findings in the six forms of autosomal recessive limb-girdle muscular dystrophies
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
