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Filtros : "Rosenberg, Carla" "Neuromuscular Disorders" Limpar

Filtros

Trabalho de evento-resumo periodico
A new form of myopathy associated with muscle hypertrophy, short stature, macroglossia and brachydactyly (2011)
Vainzof, Mariz ; Gurgel Giannetti, Juliana; Bertola, Débora Romeo; Pavanello, R C M; Oliveira, A B; Rosenberg, Carla ; Kok, F; Almeida, C. F; Martins-Bach, A. B; Zatz, Mayana
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MACROGLOSSIA, DISTROFIA MUSCULAR
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ABNT
VAINZOF, Mariz et al. A new form of myopathy associated with muscle hypertrophy, short stature, macroglossia and brachydactyly. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2011.06.834. Acesso em: 03 out. 2024. , 2011
APA
Vainzof, M., Gurgel Giannetti, J., Bertola, D. R., Pavanello, R. C. M., Oliveira, A. B., Rosenberg, C., et al. (2011). A new form of myopathy associated with muscle hypertrophy, short stature, macroglossia and brachydactyly. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2011.06.834
NLM
Vainzof M, Gurgel Giannetti J, Bertola DR, Pavanello RCM, Oliveira AB, Rosenberg C, Kok F, Almeida CF, Martins-Bach AB, Zatz M. A new form of myopathy associated with muscle hypertrophy, short stature, macroglossia and brachydactyly [Internet]. Neuromuscular Disorders. 2011 ; 21( 9): 664 res. P2.11.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.834
Vancouver
Vainzof M, Gurgel Giannetti J, Bertola DR, Pavanello RCM, Oliveira AB, Rosenberg C, Kok F, Almeida CF, Martins-Bach AB, Zatz M. A new form of myopathy associated with muscle hypertrophy, short stature, macroglossia and brachydactyly [Internet]. Neuromuscular Disorders. 2011 ; 21( 9): 664 res. P2.11.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.834
Artigo de periodico
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization (1998)
Rosenberg, Carla ; Navajas, L; Vagenas, Dulci Fonseca; Bakker, E; Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Takata, R I; Van Ommen, G J B; Zatz, Mayana ; Den Dunnen, J T
Source: Neuromuscular Disorders. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROSENBERG, Carla et al. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization. Neuromuscular Disorders, v. 8, p. 417-452, 1998Tradução . . Disponível em: https://doi.org/10.1016/s0960-8966(98)00050-9. Acesso em: 03 out. 2024.
APA
Rosenberg, C., Navajas, L., Vagenas, D. F., Bakker, E., Vainzof, M., Passos-Bueno, M. R., et al. (1998). Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization. Neuromuscular Disorders, 8, 417-452. doi:10.1016/s0960-8966(98)00050-9
NLM
Rosenberg C, Navajas L, Vagenas DF, Bakker E, Vainzof M, Passos-Bueno MR, Takata RI, Van Ommen GJB, Zatz M, Den Dunnen JT. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization [Internet]. Neuromuscular Disorders. 1998 ; 8 417-452.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/s0960-8966(98)00050-9
Vancouver
Rosenberg C, Navajas L, Vagenas DF, Bakker E, Vainzof M, Passos-Bueno MR, Takata RI, Van Ommen GJB, Zatz M, Den Dunnen JT. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization [Internet]. Neuromuscular Disorders. 1998 ; 8 417-452.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/s0960-8966(98)00050-9

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