Familial occurrence of duchenne dystrophy through paternal lines in four families (1991)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- DOI: 10.1002/ajmg.1320380118
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v.38, n.1 , p.80-4, jan. 1991
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ZATZ, Mayana et al. Familial occurrence of duchenne dystrophy through paternal lines in four families. American Journal of Medical Genetics, v. 38, n. ja 1991, p. 80-4, 1991Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320380118. Acesso em: 19 abr. 2024. -
APA
Zatz, M., Passos-Bueno, M. R., Rapaport, D., & Vainzof, M. (1991). Familial occurrence of duchenne dystrophy through paternal lines in four families. American Journal of Medical Genetics, 38( ja 1991), 80-4. doi:10.1002/ajmg.1320380118 -
NLM
Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M. Familial occurrence of duchenne dystrophy through paternal lines in four families [Internet]. American Journal of Medical Genetics. 1991 ;38( ja 1991): 80-4.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320380118 -
Vancouver
Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M. Familial occurrence of duchenne dystrophy through paternal lines in four families [Internet]. American Journal of Medical Genetics. 1991 ;38( ja 1991): 80-4.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320380118 - 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
- 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
- Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
- 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
Informações sobre o DOI: 10.1002/ajmg.1320380118 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas