Article
Publicly Available
Different approaches of molecular scanning of point mutations in genetic diseases
-
M. Ferrari
Published/Copyright:
January 1, 2009
Published Online: 2009-01-01
Published in Print: 1996-01-01
© 2013 Walter de Gruyter GmbH, Berlin/Boston
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Articles in the same Issue
- Strategies for immunoassay
- Micromachining: A new direction for clinical analyzers
- Design and implementation of a microchemistry analyzer
- Aims, objectives and work program of ISO/TC 212
- The impact of regulations, accreditation standards, and 'healthcare reform' on laboratory practice in the United States
- New initiatives in the standardization of protein measurements
- Neglected aspects in the standardization of protein measurements. A standardized comparison method
- Practical subminiature immunoanalysis
- Critical aspects in routine coagulation testing
- New developments in particle-based immunoassays: Introduction
- Determination of β2-microglobulin in human serum and urine by latex turbidimetry
- Performance of a direct LDL-cholesterol method compared to beta quantification
- The measurement of hormones and bacterial antigens using rapid particle-based immunoassays
- Isolation of hematopoietic progenitors. An approach to two different immunomagnetic methods at the lab scale
- Quantitative reticulocyte counting: Clinical applications
- Recent developments in automatic DNA sequencing
- Different approaches of molecular scanning of point mutations in genetic diseases
- Nomenclature of carbohydrates (IUPAC Recommendations 1996)