Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in duchenne muscular dystrophy (1991)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- School: IB
- DOI: 10.1002/ajmg.1320390414
- Subject: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v.39, n.4 , p.437-41, jun. 1991
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RAPAPORT, D et al. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in duchenne muscular dystrophy. American Journal of Medical Genetics, v. 39, n. ju 1991, p. 437-41, 1991Tradução . . Acesso em: 25 jun. 2022. -
APA
Rapaport, D., Passos-Bueno, M. R., Brandao, L., Love, D., Vainzof, M., & Zatz, M. (1991). Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in duchenne muscular dystrophy. American Journal of Medical Genetics, 39( ju 1991), 437-41. doi:10.1002/ajmg.1320390414 -
NLM
Rapaport D, Passos-Bueno MR, Brandao L, Love D, Vainzof M, Zatz M. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in duchenne muscular dystrophy. American Journal of Medical Genetics. 1991 ;39( ju 1991): 437-41.[citado 2022 jun. 25 ] -
Vancouver
Rapaport D, Passos-Bueno MR, Brandao L, Love D, Vainzof M, Zatz M. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in duchenne muscular dystrophy. American Journal of Medical Genetics. 1991 ;39( ju 1991): 437-41.[citado 2022 jun. 25 ] - 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
- Anticipation revisited in facioscapulohumeral muscular dystrophy
- 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
Informações sobre o DOI: 10.1002/ajmg.1320390414 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
