Search research articles
Contact Us
Filters
Showing results (51-60 of 217) with videos related to
Page
of 22
Sort By:
Human Molecular Genetics
|
June 1, 1993
Molecular diagnosis of homozygous myotonic dystrophy in two asymptomatic sisters
A Cobo, J M Martinez, L Martorell, et al.
Neurology
|
May 1, 1997
Cramps and minimal EMG abnormalities as preclinical manifestations of spinal muscular atrophy patients with homozygous deletions of the SMN gene
E Bussaglia, E F Tizzano, I Illa, et al.
Lancet (London, England)
|
March 26, 1994
Intron 22 inversions and haemophilia
E F Tizzano, C Altisent, J Tusell, et al.
European Journal of Pediatrics
|
July 1, 1994
Severe mental retardation in a young boy with an in-frame deletion in the dystrophin gene
J Colomer, P Gallano, L V Nicholson, et al.
Blood
|
June 15, 1994
Inversions in the factor VIII gene in Spanish hemophilia A patients
E F Tizzano, M Domènech, C Altisent, et al.
Journal of Medical Genetics
|
August 1, 1995
Comparison of CTG repeat length expansion and clinical progression of myotonic dystrophy over a five year period
L Martorell, J M Martinez, N Carey, et al.
The Journal of Biological Chemistry
|
January 27, 1998
Differential regulation of urokinase-type plasminogen activator expression by basic fibroblast growth factor and serum in myogenesis. Requirement of a common mitogen-activated protein kinase pathway
F Miralles, D Ron, M Baiget, et al.
Leukemia
|
January 1, 1995
Polymorphism in the RAG-1 gene identified by SSCP
J F Nomdedéu, A Lasa, R Seminago, et al.
Haematologica
|
May 18, 1999
Colorectal cancer and HFE gene mutations
A Altés, E Gimferrer, G Capella, et al.
Cancer Chemotherapy and Pharmacology
|
September 28, 2005
Methylenetetrahydrofolate reductase gene polymorphisms: genomic predictors of clinical response to fluoropyrimidine-based chemotherapy?
E Marcuello, A Altés, A Menoyo, et al.
Page
of 22
Search research articles
Search
Showing results (51-60 of 217) with videos related to
Sort By:
Page
of 22
Human Molecular Genetics
|
June 1, 1993
Molecular diagnosis of homozygous myotonic dystrophy in two asymptomatic sisters
A Cobo, J M Martinez, L Martorell, et al.
Neurology
|
May 1, 1997
Cramps and minimal EMG abnormalities as preclinical manifestations of spinal muscular atrophy patients with homozygous deletions of the SMN gene
E Bussaglia, E F Tizzano, I Illa, et al.
Lancet (London, England)
|
March 26, 1994
Intron 22 inversions and haemophilia
E F Tizzano, C Altisent, J Tusell, et al.
European Journal of Pediatrics
|
July 1, 1994
Severe mental retardation in a young boy with an in-frame deletion in the dystrophin gene
J Colomer, P Gallano, L V Nicholson, et al.
Blood
|
June 15, 1994
Inversions in the factor VIII gene in Spanish hemophilia A patients
E F Tizzano, M Domènech, C Altisent, et al.
Journal of Medical Genetics
|
August 1, 1995
Comparison of CTG repeat length expansion and clinical progression of myotonic dystrophy over a five year period
L Martorell, J M Martinez, N Carey, et al.
The Journal of Biological Chemistry
|
January 27, 1998
Differential regulation of urokinase-type plasminogen activator expression by basic fibroblast growth factor and serum in myogenesis. Requirement of a common mitogen-activated protein kinase pathway
F Miralles, D Ron, M Baiget, et al.
Leukemia
|
January 1, 1995
Polymorphism in the RAG-1 gene identified by SSCP
J F Nomdedéu, A Lasa, R Seminago, et al.
Haematologica
|
May 18, 1999
Colorectal cancer and HFE gene mutations
A Altés, E Gimferrer, G Capella, et al.
Cancer Chemotherapy and Pharmacology
|
September 28, 2005
Methylenetetrahydrofolate reductase gene polymorphisms: genomic predictors of clinical response to fluoropyrimidine-based chemotherapy?
E Marcuello, A Altés, A Menoyo, et al.
Page
of 22