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M R Passos

Showing results (61-70 of 142) with videos related to

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Journal of the Neurological Sciences|May 1, 1991
Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophiesM R Passos-Bueno, M Vainzof, R de C Pavanello, et al.
Neuromuscular Disorders : NMD|July 16, 2002
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?M M O Tonini, M R Passos-Bueno, A Cerqueira, et al.
Journal of Medical Genetics|March 1, 1990
Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115M R Passos-Bueno, D Rapaport, D Love, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The phenotype of chromosome 2p-linked limb-girdle muscular dystrophyI Mahjneh, M R Passos-Bueno, M Zatz, et al.
Journal of Medical Genetics|February 5, 2003
Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutationsE S Moreira, M Vainzof, O T Suzuki, et al.
American Journal of Medical Genetics|August 15, 1994
Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritanceM R Passos-Bueno, S K Marie, M Monteiro, et al.
Human Mutation|January 1, 1997
Novel point mutations in the dystrophin geneR Sitnik, S Campiotto, M Vainzof, et al.
Human Molecular Genetics|June 1, 1996
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3A L Sertié, M Quimby, E S Moreira, et al.
Journal of the Neurological Sciences|May 1, 1994
Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophyM Zatz, K Matsumura, M Vainzof, et al.
Journal of the Neurological Sciences|September 1, 1990
Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian studyM Vainzof, R C Pavanello, I Pavanello Filho, et al.
Pageof 15

Showing results (61-70 of 142) with videos related to

Sort By:
Pageof 15
Journal of the Neurological Sciences|May 1, 1991
Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophiesM R Passos-Bueno, M Vainzof, R de C Pavanello, et al.
Neuromuscular Disorders : NMD|July 16, 2002
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?M M O Tonini, M R Passos-Bueno, A Cerqueira, et al.
Journal of Medical Genetics|March 1, 1990
Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115M R Passos-Bueno, D Rapaport, D Love, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The phenotype of chromosome 2p-linked limb-girdle muscular dystrophyI Mahjneh, M R Passos-Bueno, M Zatz, et al.
Journal of Medical Genetics|February 5, 2003
Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutationsE S Moreira, M Vainzof, O T Suzuki, et al.
American Journal of Medical Genetics|August 15, 1994
Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritanceM R Passos-Bueno, S K Marie, M Monteiro, et al.
Human Mutation|January 1, 1997
Novel point mutations in the dystrophin geneR Sitnik, S Campiotto, M Vainzof, et al.
Human Molecular Genetics|June 1, 1996
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3A L Sertié, M Quimby, E S Moreira, et al.
Journal of the Neurological Sciences|May 1, 1994
Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophyM Zatz, K Matsumura, M Vainzof, et al.
Journal of the Neurological Sciences|September 1, 1990
Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian studyM Vainzof, R C Pavanello, I Pavanello Filho, et al.
Pageof 15