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M R Passos

Showing results (51-60 of 142) with videos related to

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American Journal of Medical Genetics|May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than femalesM Zatz, S K Marie, A Cerqueira, et al.
American Journal of Medical Genetics|August 26, 1998
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial casesM Zatz, D Sumita, S Campiotto, et al.
Neuromuscular Disorders : NMD|December 9, 2003
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)M M O Tonini, M R Passos-Bueno, A Cerqueira, et al.
American Journal of Human Genetics|July 1, 1997
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12E S Moreira, M Vainzof, S K Marie, et al.
Human Heredity|January 1, 1991
Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophiesE Rabbi-Bortolini, G M Dal Colletto, M R Passos-Bueno, et al.
Revista Paulista De Medicina|November 1, 1985
[Placental alkaline phosphatase levels in serum of pregnant women: study in Salvador, Bahia]M C Silva, M R Passos-Bueno, G Sousa M das, et al.
Journal of the Neurological Sciences|June 29, 1999
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationM Vainzof, M R Passos-Bueno, R C Pavanello, et al.
American Journal of Medical Genetics|April 17, 1998
Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosisE Rabbi-Bortolini, A L Bernardino, A L Lopes, et al.
Human Mutation|July 29, 1999
Clinical spectrum of fibroblast growth factor receptor mutationsM R Passos-Bueno, W R Wilcox, E W Jabs, et al.
American Journal of Medical Genetics|January 1, 1991
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequenceM R Passos-Bueno, J Terwilliger, J Ott, et al.
Pageof 15

Showing results (51-60 of 142) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics|May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than femalesM Zatz, S K Marie, A Cerqueira, et al.
American Journal of Medical Genetics|August 26, 1998
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial casesM Zatz, D Sumita, S Campiotto, et al.
Neuromuscular Disorders : NMD|December 9, 2003
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)M M O Tonini, M R Passos-Bueno, A Cerqueira, et al.
American Journal of Human Genetics|July 1, 1997
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12E S Moreira, M Vainzof, S K Marie, et al.
Human Heredity|January 1, 1991
Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophiesE Rabbi-Bortolini, G M Dal Colletto, M R Passos-Bueno, et al.
Revista Paulista De Medicina|November 1, 1985
[Placental alkaline phosphatase levels in serum of pregnant women: study in Salvador, Bahia]M C Silva, M R Passos-Bueno, G Sousa M das, et al.
Journal of the Neurological Sciences|June 29, 1999
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationM Vainzof, M R Passos-Bueno, R C Pavanello, et al.
American Journal of Medical Genetics|April 17, 1998
Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosisE Rabbi-Bortolini, A L Bernardino, A L Lopes, et al.
Human Mutation|July 29, 1999
Clinical spectrum of fibroblast growth factor receptor mutationsM R Passos-Bueno, W R Wilcox, E W Jabs, et al.
American Journal of Medical Genetics|January 1, 1991
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequenceM R Passos-Bueno, J Terwilliger, J Ott, et al.
Pageof 15