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M R Passos

Showing results (41-50 of 142) with videos related to

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Journal of the Neurological Sciences|October 1, 1993
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotypeM Vainzof, M R Passos-Bueno, R I Takata, et al.
Memorias Do Instituto Oswaldo Cruz|April 1, 1994
Human papillomavirus detection in genital lesions by in situ hybridization and ultrastructural observationsL H Oliveira, I C Frugulhetti, M R Passos, et al.
American Journal of Medical Genetics|September 5, 2002
Further evidence for a fourth gene causing X-linked pure spastic paraplegiaA Starling, P Rocco, F Cambi, et al.
Memorias Do Instituto Oswaldo Cruz|October 1, 1994
Prevalence of human papillomavirus DNA in female cervical lesions from Rio de Janeiro, BrazilS M Cavalcanti, I C Frugulhetti, M R Passos, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complexM Vainzof, E S Moreira, G Ferraz, et al.
Human Biology|April 1, 1991
Null allele in a human polymorphism restricted to the placenta: call for a searchM C Silva, M G Sousa, R D Carvalho, et al.
Human Molecular Genetics|March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Human Molecular Genetics|August 15, 2000
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)A L Sertié, V Sossi, A A Camargo, et al.
American Journal of Medical Genetics|October 1, 1992
Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern of DNA deletionM Vainzof, M R Passos-Bueno, D Rapaport, et al.
Journal of Medical Genetics|December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathiesE S Moreira, M Vainzof, S K Marie, et al.
Pageof 15

Showing results (41-50 of 142) with videos related to

Sort By:
Pageof 15
Journal of the Neurological Sciences|October 1, 1993
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotypeM Vainzof, M R Passos-Bueno, R I Takata, et al.
Memorias Do Instituto Oswaldo Cruz|April 1, 1994
Human papillomavirus detection in genital lesions by in situ hybridization and ultrastructural observationsL H Oliveira, I C Frugulhetti, M R Passos, et al.
American Journal of Medical Genetics|September 5, 2002
Further evidence for a fourth gene causing X-linked pure spastic paraplegiaA Starling, P Rocco, F Cambi, et al.
Memorias Do Instituto Oswaldo Cruz|October 1, 1994
Prevalence of human papillomavirus DNA in female cervical lesions from Rio de Janeiro, BrazilS M Cavalcanti, I C Frugulhetti, M R Passos, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complexM Vainzof, E S Moreira, G Ferraz, et al.
Human Biology|April 1, 1991
Null allele in a human polymorphism restricted to the placenta: call for a searchM C Silva, M G Sousa, R D Carvalho, et al.
Human Molecular Genetics|March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Human Molecular Genetics|August 15, 2000
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)A L Sertié, V Sossi, A A Camargo, et al.
American Journal of Medical Genetics|October 1, 1992
Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern of DNA deletionM Vainzof, M R Passos-Bueno, D Rapaport, et al.
Journal of Medical Genetics|December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathiesE S Moreira, M Vainzof, S K Marie, et al.
Pageof 15