Search research articles
Contact Us
Filters
Showing results (111-120 of 142) with videos related to
Page
of 15
Sort By:
Journal of Medical Genetics
|
June 28, 2005
Decreased cellular uptake and metabolism in Allan-Herndon-Dudley syndrome (AHDS) due to a novel mutation in the MCT8 thyroid hormone transporter
C M C Maranduba, E C H Friesema, F Kok, et al.
Journal of Medical Virology
|
June 26, 2010
Clinical evaluation of the NS1 antigen-capture ELISA for early diagnosis of dengue virus infection in Brazil
Luiza A Castro-Jorge, Paula R L Machado, Camila A Fávero, et al.
American Journal of Medical Genetics
|
February 27, 1995
Becker and limb-girdle muscular dystrophies: a psychiatric and intellectual level comparative study
M Melo, V Lauriano, V Gentil, et al.
Journal of Molecular Neuroscience : MN
|
October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophies
M Vainzof, L V Anderson, E M McNally, et al.
American Journal of Medical Genetics
|
April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
M R Passos-Bueno, B C Byth, S Rosenberg, et al.
Annals of Neurology
|
August 1, 1997
Familial spongiform encephalopathy associated with a novel prion protein gene mutation
R Nitrini, S Rosemberg, M R Passos-Bueno, et al.
Molecular Psychiatry
|
March 24, 1999
The association of the short variant of the 5-HTTPLR polymorphism and the apoE epsilon4 allele does not increase the risk for late onset Alzheimer's disease
J R Oliveira, C M Shimokomaki, P R Brito-Marques, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
July 16, 2008
Association of polymorphisms at the ADIPOR1 regulatory region with type 2 diabetes and body mass index in a Brazilian population with European or African ancestry
E Yeh, L Kimura, F I V Errera, et al.
Nature Genetics
|
February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin
E S Moreira, T J Wiltshire, G Faulkner, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization
C Rosenberg, L Navajas, D F Vagenas, et al.
Page
of 15
Search research articles
Search
Showing results (111-120 of 142) with videos related to
Sort By:
Page
of 15
Journal of Medical Genetics
|
June 28, 2005
Decreased cellular uptake and metabolism in Allan-Herndon-Dudley syndrome (AHDS) due to a novel mutation in the MCT8 thyroid hormone transporter
C M C Maranduba, E C H Friesema, F Kok, et al.
Journal of Medical Virology
|
June 26, 2010
Clinical evaluation of the NS1 antigen-capture ELISA for early diagnosis of dengue virus infection in Brazil
Luiza A Castro-Jorge, Paula R L Machado, Camila A Fávero, et al.
American Journal of Medical Genetics
|
February 27, 1995
Becker and limb-girdle muscular dystrophies: a psychiatric and intellectual level comparative study
M Melo, V Lauriano, V Gentil, et al.
Journal of Molecular Neuroscience : MN
|
October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophies
M Vainzof, L V Anderson, E M McNally, et al.
American Journal of Medical Genetics
|
April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
M R Passos-Bueno, B C Byth, S Rosenberg, et al.
Annals of Neurology
|
August 1, 1997
Familial spongiform encephalopathy associated with a novel prion protein gene mutation
R Nitrini, S Rosemberg, M R Passos-Bueno, et al.
Molecular Psychiatry
|
March 24, 1999
The association of the short variant of the 5-HTTPLR polymorphism and the apoE epsilon4 allele does not increase the risk for late onset Alzheimer's disease
J R Oliveira, C M Shimokomaki, P R Brito-Marques, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
July 16, 2008
Association of polymorphisms at the ADIPOR1 regulatory region with type 2 diabetes and body mass index in a Brazilian population with European or African ancestry
E Yeh, L Kimura, F I V Errera, et al.
Nature Genetics
|
February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin
E S Moreira, T J Wiltshire, G Faulkner, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization
C Rosenberg, L Navajas, D F Vagenas, et al.
Page
of 15