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: 13 maio 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 maio 13 ] -
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 maio 13 ] - 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
- Associacao do retardo mental com delecoes dos exons 50 a 54 do gene da distrofina em pacientes com distrofia muscular tipo duchenne
- Estudos de ligação em famílias com ataxia espinocerebelar
- Localizacao de genes responsaveis pelas distrofias musculares tipo cinturas atraves de microsatelites
- Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk
- Use of polymerase chain reaction (pcr) for diagnosis of duchenne muscular dystrophy (dmd)
- Understanding the molecular biology of chromosome 2p-linked lgmd (lgmd 2b)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas