Search for a diagnostic test
Diagnosis of familial hyperaldosteronism type 1 (CYP11B1 gene: sequencing)
Despite our efforts to ensure that data is up to date, this activity has not been validated since 07/11/2014- Pränatal-Medizin München, Frauenärzte und Humangenetiker, Labor für molekulare Genetik
- Pränatal-Medizin München MVZ GmbH
- Aiblingerstr. 8
- 80639 MÜNCHEN
- GERMANY
- Director of laboratory : Dr Christoph BAGOWSKI
- More information
Last update: November 2014
Responsible of diagnostic test
Purpose(s)
Post-natal diagnosis
Technical procedure(s)
Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
List of diseases and genes
List of diseases tested
(1)
List of genes tested (including panels)
(1)
Additional information
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.