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M R Passos

Showing results (91-100 of 142) with videos related to

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Genetic Epidemiology|November 15, 2002
Evidence that BCL3 plays a role in the etiology of nonsyndromic oral clefts in Brazilian familiesD A Gaspar, S R Matioli, R C Pavanello, et al.
Nature Genetics|October 1, 1996
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan geneV Nigro, E de Sá Moreira, G Piluso, et al.
Neuromuscular Disorders : NMD|January 1, 1992
A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardationD Rapaport, M R Passos-Bueno, R I Takata, et al.
Molecular Psychiatry|January 14, 2015
Altered mTORC1 signaling in multipotent stem cells from nearly 25% of patients with nonsyndromic autism spectrum disordersA M Suzuki, K Griesi-Oliveira, C de Oliveira Freitas Machado, et al.
American Journal of Medical Genetics|April 1, 1991
Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studiesM Vainzof, R C Pavanello, I Pavanello-Filho, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1994
[Myotonic dystrophy: study of clinico-genetic correlation in a pair of relatives (father-son)]U C Reed, M R Passos-Bueno, S K Nagahashi-Marie, et al.
Human Molecular Genetics|February 1, 1993
Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive Duchenne-like muscular dystrophy in Brazilian familiesM R Passos-Bueno, E Bakker, S K Marie, et al.
Journal of Medical Genetics|May 1, 1993
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian familiesM R Passos-Bueno, I Richard, M Vainzof, et al.
Human Molecular Genetics|November 1, 1993
Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysisM R Passos-Bueno, J R Oliveira, E Bakker, et al.
Genomics|May 1, 1995
Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate regionM R Passos-Bueno, R Bashir, E S Moreira, et al.
Pageof 15

Showing results (91-100 of 142) with videos related to

Sort By:
Pageof 15
Genetic Epidemiology|November 15, 2002
Evidence that BCL3 plays a role in the etiology of nonsyndromic oral clefts in Brazilian familiesD A Gaspar, S R Matioli, R C Pavanello, et al.
Nature Genetics|October 1, 1996
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan geneV Nigro, E de Sá Moreira, G Piluso, et al.
Neuromuscular Disorders : NMD|January 1, 1992
A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardationD Rapaport, M R Passos-Bueno, R I Takata, et al.
Molecular Psychiatry|January 14, 2015
Altered mTORC1 signaling in multipotent stem cells from nearly 25% of patients with nonsyndromic autism spectrum disordersA M Suzuki, K Griesi-Oliveira, C de Oliveira Freitas Machado, et al.
American Journal of Medical Genetics|April 1, 1991
Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studiesM Vainzof, R C Pavanello, I Pavanello-Filho, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1994
[Myotonic dystrophy: study of clinico-genetic correlation in a pair of relatives (father-son)]U C Reed, M R Passos-Bueno, S K Nagahashi-Marie, et al.
Human Molecular Genetics|February 1, 1993
Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive Duchenne-like muscular dystrophy in Brazilian familiesM R Passos-Bueno, E Bakker, S K Marie, et al.
Journal of Medical Genetics|May 1, 1993
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian familiesM R Passos-Bueno, I Richard, M Vainzof, et al.
Human Molecular Genetics|November 1, 1993
Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysisM R Passos-Bueno, J R Oliveira, E Bakker, et al.
Genomics|May 1, 1995
Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate regionM R Passos-Bueno, R Bashir, E S Moreira, et al.
Pageof 15