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Publications by Deborah Barden
Diagnosis of Five Spinocerebellar Ataxia Disorders by Multiplex Amplification and Capillary Electrophoresis
Journal of Molecular Diagnostics
Forensic Medicine
Pathology
Molecular Medicine
Related publications
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
Spinocerebellar Ataxia Type 13
Spinocerebellar Ataxia Type 3
Spinocerebellar Ataxia Type 8
Spinocerebellar Ataxia Type 12
Spinocerebellar Ataxia Type 37
Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 40
Spinocerebellar Ataxia Type 31
Clinical Neurology
Neurology