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EJIFCC
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September 30, 2016
2. Post-Natal Molecular Diagnosis of Inherited Diseases
Maurizio Ferrari, Laura Cremonesi, Stefania Stenirri
EJIFCC
|
September 30, 2016
10. Circulating Nucleic Acids as Diagnostic Tool
Maurizio Ferrari, Laura Cremonesi, Silvia Galbiati
Clinical Chemistry and Laboratory Medicine
|
May 16, 2003
Molecular diagnostics by microelectronic microchips
Maurizio Ferrari, Stefania Stenirri, Pierangelo Bonini, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
April 22, 2008
A fast microelectronic array for screening and prenatal diagnosis of beta-thalassemia
Barbara Foglieni, Silvia Galbiati, Maurizio Ferrari, et al.
Methods in Molecular Medicine
|
September 15, 2005
Single-nucleotide polymorphism and mutation identification by the nanogen microelectronic chip technology
Maurizio Ferrari, Laura Cremonesi, Pierangelo Bonini, et al.
Expert Review of Molecular Diagnostics
|
April 19, 2005
Molecular diagnostics by microelectronic microchips
Maurizio Ferrari, Laura Cremonesi, Pierangelo Bonini, et al.
Haematologica
|
December 17, 2009
The -582A>G variant of the HAMP promoter is not associated with high serum ferritin levels in normal subjects
Francesca Bruno, Sara Bonalumi, Clara Camaschella, et al.
Electrophoresis
|
November 28, 2007
High-throughput mutational screening for beta-thalassemia by single-nucleotide extension
Silvia Galbiati, Marcella Chiari, Micol Macellari, et al.
Electrophoresis
|
December 5, 2008
Development of new substrates for high-sensitive genotyping of minority mutated alleles
Silvia Galbiati, Francesco Damin, Gabriele Di Carlo, et al.
Medical Decision Making : an International Journal of the Society for Medical Decision Making
|
April 23, 2011
The 1-in-X effect on the subjective assessment of medical probabilities
Stefania Pighin, Lucia Savadori, Elisa Barilli, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 65) with videos related to
Sort By:
Page
of 7
EJIFCC
|
September 30, 2016
2. Post-Natal Molecular Diagnosis of Inherited Diseases
Maurizio Ferrari, Laura Cremonesi, Stefania Stenirri
EJIFCC
|
September 30, 2016
10. Circulating Nucleic Acids as Diagnostic Tool
Maurizio Ferrari, Laura Cremonesi, Silvia Galbiati
Clinical Chemistry and Laboratory Medicine
|
May 16, 2003
Molecular diagnostics by microelectronic microchips
Maurizio Ferrari, Stefania Stenirri, Pierangelo Bonini, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
April 22, 2008
A fast microelectronic array for screening and prenatal diagnosis of beta-thalassemia
Barbara Foglieni, Silvia Galbiati, Maurizio Ferrari, et al.
Methods in Molecular Medicine
|
September 15, 2005
Single-nucleotide polymorphism and mutation identification by the nanogen microelectronic chip technology
Maurizio Ferrari, Laura Cremonesi, Pierangelo Bonini, et al.
Expert Review of Molecular Diagnostics
|
April 19, 2005
Molecular diagnostics by microelectronic microchips
Maurizio Ferrari, Laura Cremonesi, Pierangelo Bonini, et al.
Haematologica
|
December 17, 2009
The -582A>G variant of the HAMP promoter is not associated with high serum ferritin levels in normal subjects
Francesca Bruno, Sara Bonalumi, Clara Camaschella, et al.
Electrophoresis
|
November 28, 2007
High-throughput mutational screening for beta-thalassemia by single-nucleotide extension
Silvia Galbiati, Marcella Chiari, Micol Macellari, et al.
Electrophoresis
|
December 5, 2008
Development of new substrates for high-sensitive genotyping of minority mutated alleles
Silvia Galbiati, Francesco Damin, Gabriele Di Carlo, et al.
Medical Decision Making : an International Journal of the Society for Medical Decision Making
|
April 23, 2011
The 1-in-X effect on the subjective assessment of medical probabilities
Stefania Pighin, Lucia Savadori, Elisa Barilli, et al.
Page
of 7