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Publications by M. Esther Farez-Vidal
Multiplex Analysis of the Most Common Mutations Related to Hereditary Haemochromatosis: Two Methods Combining Specific Amplification With Capillary Electrophoresis
European Journal of Haematology
Medicine
Hematology
Related publications
Diagnosis of Five Spinocerebellar Ataxia Disorders by Multiplex Amplification and Capillary Electrophoresis
Journal of Molecular Diagnostics
Forensic Medicine
Pathology
Molecular Medicine
Hereditary (Primary) Haemochromatosis.
BMJ
Hereditary (Primary) Haemochromatosis.
BMJ
Detection of FLT3 Internal Tandem Duplication and D835 Mutations by a Multiplex Polymerase Chain Reaction and Capillary Electrophoresis Assay
Journal of Molecular Diagnostics
Forensic Medicine
Pathology
Molecular Medicine
Application of Capillary Electrophoresis With Sensitive Detection to Analysis for Saccharide Molecules.
Analytical Sciences
Analytical Chemistry
Identification of the Most Common Pathogenic Bacteria in Patients With Suspected Sepsis by Multiplex PCR
Journal of Infection in Developing Countries
Medicine
Virology
Parasitology
Infectious Diseases
Microbiology
Capillary Electrophoresis
Use of Capillary Electrophoresis for Microbial Analysis
Capillary Electrophoresis
