Evidence of further genetic heterogeneity for both autosomal dominant and autosomal recessive limb-girdle muscular dystrophy (2001)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Assunto: DISTROFIA MUSCULAR
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Human Genetics
- Volume/Número/Paginação/Ano: v. 69, n. 4, suppl., p. 513, oct. 2001
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
ABNT
STARLING, A. L. et al. Evidence of further genetic heterogeneity for both autosomal dominant and autosomal recessive limb-girdle muscular dystrophy. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 jun. 2024. , 2001 -
APA
Starling, A. L., Vainzof, M., Pavanello, R. de C. M., Canovas, M., Cerqueira, A., Passos-Bueno, M. R., & Zatz, M. (2001). Evidence of further genetic heterogeneity for both autosomal dominant and autosomal recessive limb-girdle muscular dystrophy. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. -
NLM
Starling AL, Vainzof M, Pavanello R de CM, Canovas M, Cerqueira A, Passos-Bueno MR, Zatz M. Evidence of further genetic heterogeneity for both autosomal dominant and autosomal recessive limb-girdle muscular dystrophy. American Journal of Human Genetics. 2001 ; 69( 4): 513.[citado 2024 jun. 01 ] -
Vancouver
Starling AL, Vainzof M, Pavanello R de CM, Canovas M, Cerqueira A, Passos-Bueno MR, Zatz M. Evidence of further genetic heterogeneity for both autosomal dominant and autosomal recessive limb-girdle muscular dystrophy. American Journal of Human Genetics. 2001 ; 69( 4): 513.[citado 2024 jun. 01 ] - 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
