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Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
July 25, 2006
Effect of polymorphisms of the MTHFR and APOE genes on susceptibility to diabetes and severity of diabetic retinopathy in Brazilian patients
F I V Errera, M E R Silva, E Yeh, et al.
Human Molecular Genetics
|
December 1, 1996
Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)
C G Bönnemann, M R Passos-Bueno, E M McNally, et al.
Infectious Diseases in Obstetrics and Gynecology
|
August 14, 1998
Vulvar myiasis
M R Passos, A V Carvalho, A L Dutra, et al.
Journal of Medical Genetics
|
June 14, 2008
New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome
G de Alencastro, D E McCloskey, S E Kliemann, et al.
Journal of Medical Genetics
|
February 1, 1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families
M R Passos-Bueno, E S Moreira, S K Marie, et al.
Human Molecular Genetics
|
December 1, 1996
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies
M Vainzof, M R Passos-Bueno, M Canovas, et al.
American Journal of Human Genetics
|
November 5, 2002
Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome
O T Suzuki, A L Sertié, V M Der Kaloustian, et al.
American Journal of Human Genetics
|
November 1, 1996
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation
E M McNally, M R Passos-Bueno, C G Bönnemann, et al.
Human Molecular Genetics
|
May 23, 1998
Caveolin-3 in muscular dystrophy
E M McNally, E de Sá Moreira, D J Duggan, et al.
Clinical Genetics
|
November 8, 2017
Richieri-Costa-Pereira syndrome: Expanding its phenotypic and genotypic spectrum
D R Bertola, G Hsia, L Alvizi, et al.
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of 15
Search research articles
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Showing results (121-130 of 142) with videos related to
Sort By:
Page
of 15
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
July 25, 2006
Effect of polymorphisms of the MTHFR and APOE genes on susceptibility to diabetes and severity of diabetic retinopathy in Brazilian patients
F I V Errera, M E R Silva, E Yeh, et al.
Human Molecular Genetics
|
December 1, 1996
Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)
C G Bönnemann, M R Passos-Bueno, E M McNally, et al.
Infectious Diseases in Obstetrics and Gynecology
|
August 14, 1998
Vulvar myiasis
M R Passos, A V Carvalho, A L Dutra, et al.
Journal of Medical Genetics
|
June 14, 2008
New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome
G de Alencastro, D E McCloskey, S E Kliemann, et al.
Journal of Medical Genetics
|
February 1, 1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families
M R Passos-Bueno, E S Moreira, S K Marie, et al.
Human Molecular Genetics
|
December 1, 1996
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies
M Vainzof, M R Passos-Bueno, M Canovas, et al.
American Journal of Human Genetics
|
November 5, 2002
Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome
O T Suzuki, A L Sertié, V M Der Kaloustian, et al.
American Journal of Human Genetics
|
November 1, 1996
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation
E M McNally, M R Passos-Bueno, C G Bönnemann, et al.
Human Molecular Genetics
|
May 23, 1998
Caveolin-3 in muscular dystrophy
E M McNally, E de Sá Moreira, D J Duggan, et al.
Clinical Genetics
|
November 8, 2017
Richieri-Costa-Pereira syndrome: Expanding its phenotypic and genotypic spectrum
D R Bertola, G Hsia, L Alvizi, et al.
Page
of 15