Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? (2002)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; VAINZOF, MARIZ - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- DOI: 10.1016/s0960-8966(02)00014-7
- Assunto: DISTROFIA MUSCULAR
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Neuromuscular Disorders
- ISSN: 0960-8966
- Volume/Número/Paginação/Ano: v. 12, n. 6, p. 554-557, 2002
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
TONINI, M. M. O. et al. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?. Neuromuscular Disorders, v. 12, n. 6, p. 554-557, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0960-8966(02)00014-7. Acesso em: 23 abr. 2024. -
APA
Tonini, M. M. O., Passos-Bueno, M. R., Cerqueira, A., Pavanello, R. de C. M., Vainzof, M., Dubowitz, V., & Zatz, M. (2002). Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? Neuromuscular Disorders, 12( 6), 554-557. doi:10.1016/s0960-8966(02)00014-7 -
NLM
Tonini MMO, Passos-Bueno MR, Cerqueira A, Pavanello R de CM, Vainzof M, Dubowitz V, Zatz M. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? [Internet]. Neuromuscular Disorders. 2002 ; 12( 6): 554-557.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/s0960-8966(02)00014-7 -
Vancouver
Tonini MMO, Passos-Bueno MR, Cerqueira A, Pavanello R de CM, Vainzof M, Dubowitz V, Zatz M. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? [Internet]. Neuromuscular Disorders. 2002 ; 12( 6): 554-557.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/s0960-8966(02)00014-7 - Severe Nonspecific X-Linked Mental Retardation Caused by a-Proximally Xp Located Gene: intragenic Heterogeneity or a New Form of X-Linked Mental Retardation?
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Informações sobre o DOI: 10.1016/s0960-8966(02)00014-7 (Fonte: oaDOI API)
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