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
- School: IB
- DOI: 10.1002/ajmg.1320380118
- Subject: 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, M; PASSOS-BUENO, M R; RAPAPORT, D; VAINZOF, M. Familial occurrence of duchenne dystrophy through paternal lines in four families. American Journal of Medical Genetics, New York, v. 38, n. ja 1991, p. 80-4, 1991. DOI: 10.1002/ajmg.1320380118. -
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. American Journal of Medical Genetics. 1991 ;38( ja 1991): 80-4. -
Vancouver
Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M. Familial occurrence of duchenne dystrophy through paternal lines in four families. American Journal of Medical Genetics. 1991 ;38( ja 1991): 80-4. - Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
- Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
- Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation
- Localizacao de genes responsaveis pelas distrofias musculares tipo cinturas atraves de microsatelites
- Use of polymerase chain reaction (pcr) for diagnosis of duchenne muscular dystrophy (dmd)
- Comparison of dystrophin analyses in patients with duchenne muscular dystrophy (dmd) by immunofluorescence (if) and western-blot (wb) tecniques
- Unexpected findings in a large study of brazilian patients with xp21 muscular dystrophies
- Dystrophin abnormalities in muscle from becker muscular dystrophy (bmd) carriers
- Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk
Informações sobre o DOI: 10.1002/ajmg.1320380118 (Fonte: oaDOI API)
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