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M Baiget

Showing results (51-60 of 217) with videos related to

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Human Molecular Genetics|June 1, 1993
Molecular diagnosis of homozygous myotonic dystrophy in two asymptomatic sistersA 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 geneE Bussaglia, E F Tizzano, I Illa, et al.
Lancet (London, England)|March 26, 1994
Intron 22 inversions and haemophiliaE 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 geneJ Colomer, P Gallano, L V Nicholson, et al.
Blood|June 15, 1994
Inversions in the factor VIII gene in Spanish hemophilia A patientsE 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 periodL 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 pathwayF Miralles, D Ron, M Baiget, et al.
Leukemia|January 1, 1995
Polymorphism in the RAG-1 gene identified by SSCPJ F Nomdedéu, A Lasa, R Seminago, et al.
Haematologica|May 18, 1999
Colorectal cancer and HFE gene mutationsA 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.
Pageof 22

Showing results (51-60 of 217) with videos related to

Sort By:
Pageof 22
Human Molecular Genetics|June 1, 1993
Molecular diagnosis of homozygous myotonic dystrophy in two asymptomatic sistersA 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 geneE Bussaglia, E F Tizzano, I Illa, et al.
Lancet (London, England)|March 26, 1994
Intron 22 inversions and haemophiliaE 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 geneJ Colomer, P Gallano, L V Nicholson, et al.
Blood|June 15, 1994
Inversions in the factor VIII gene in Spanish hemophilia A patientsE 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 periodL 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 pathwayF Miralles, D Ron, M Baiget, et al.
Leukemia|January 1, 1995
Polymorphism in the RAG-1 gene identified by SSCPJ F Nomdedéu, A Lasa, R Seminago, et al.
Haematologica|May 18, 1999
Colorectal cancer and HFE gene mutationsA 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.
Pageof 22