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Diagnosis of Familial Hyperaldosteronism type I and III (CYP11B1/CYP11B2 fusion gene and KCNJ5 gene)
- Laboratorium voor Genoomdiagnostiek
- Afdeling Klinische Genetica
- Amsterdam UMC, locatie AMC
- Meibergdreef 9
- 1105 AZ AMSTERDAM
- NETHERLANDS
- Director of laboratory : Pr M.M.A.M. [Marcel] MANNENS
- More information
Last update: November 2018
Responsible of diagnostic test
Purpose(s)
Antenatal diagnosis
Post-natal diagnosis
Technical procedure(s)
Molecular genetics
Targeted mutation analysis
Sanger sequencing
Targeted mutation analysis
MLPA based techniques
Sequence analysis: entire coding region
Sanger sequencing
List of diseases and genes
List of diseases tested
(2)
Additional information
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