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Human Molecular Genetics
|
January 1, 1993
Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?
M Vainzof, R I Takata, M R Passos-Bueno, et al.
American Journal of Medical Genetics
|
March 17, 2001
Mutations in the caveolin-3 gene: When are they pathogenic?
F de Paula, M Vainzof, A L Bernardino, et al.
Journal of the Neurological Sciences
|
October 1, 1993
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype
M Vainzof, M R Passos-Bueno, R I Takata, 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 complex
M Vainzof, E S Moreira, G Ferraz, 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.
Muscle & Nerve
|
May 8, 2002
Lack of the C-terminal domain of nebulin in a patient with nemaline myopathy
J Gurgel-Giannetti, M-L Bang, U Reed, 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 sarcoglycanopathies
E S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics
|
May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females
M 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 cases
M Zatz, D Sumita, S Campiotto, et al.
American Journal of Human Genetics
|
July 1, 1997
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12
E S Moreira, M Vainzof, S K Marie, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 85) with videos related to
Sort By:
Page
of 9
Human Molecular Genetics
|
January 1, 1993
Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?
M Vainzof, R I Takata, M R Passos-Bueno, et al.
American Journal of Medical Genetics
|
March 17, 2001
Mutations in the caveolin-3 gene: When are they pathogenic?
F de Paula, M Vainzof, A L Bernardino, et al.
Journal of the Neurological Sciences
|
October 1, 1993
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype
M Vainzof, M R Passos-Bueno, R I Takata, 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 complex
M Vainzof, E S Moreira, G Ferraz, 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.
Muscle & Nerve
|
May 8, 2002
Lack of the C-terminal domain of nebulin in a patient with nemaline myopathy
J Gurgel-Giannetti, M-L Bang, U Reed, 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 sarcoglycanopathies
E S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics
|
May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females
M 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 cases
M Zatz, D Sumita, S Campiotto, et al.
American Journal of Human Genetics
|
July 1, 1997
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12
E S Moreira, M Vainzof, S K Marie, et al.
Page
of 9